Tabular[<|"RawSchema" -> <|"ColumnProperties" -> <|"CHROM" -> <|"ElementType" -> "String"|>, "POS" -> <|"ElementType" -> "Integer64"|>, "ID" -> <|"ElementType" -> "String"|>, "REF" -> <|"ElementType" -> "String"|>, "ALT" -> <|"ElementType" -> "String"|>, "QUAL" -> <|"ElementType" -> "String"|>, "FILTER" -> <|"ElementType" -> "String"|>, "INFO" -> <|"ElementType" -> "String"|>|>, "KeyColumns" -> None, "Backend" -> "WolframKernel"|>, "BackendData" -> <|"ColumnData" -> DataStructure["ColumnTable", {{TabularColumn[Association["Data" -> {{3, {0, 2, 4, 6, 8, 10, 12, 14, 16, 18, 20}, "21212121212121212121"}, {}, None}, "ElementType" -> "String"]], TabularColumn[Association["Data" -> {{6116503, 6493118, 6562008, 6562236, 7819485, 10541121, 10541137, 10552695, 10561044, 10561201}, {}, None}, "ElementType" -> "Integer64"]], TabularColumn[Association["Data" -> {{3, {0, 6, 13, 20, 27, 34, 40, 47, 54, 61, 67}, "4331403354259335850233528643356396713837233348723616612214242791664"}, {}, None}, "ElementType" -> "String"]], TabularColumn[Association["Data" -> {{3, {0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10}, "CGCCGGGCTA"}, {}, None}, "ElementType" -> "String"]], TabularColumn[Association["Data" -> {{3, {0, 1, 3, 4, 5, 6, 7, 8, 9, 10, 11}, "TGATTATCGCG"}, {}, None}, "ElementType" -> "String"]], TabularColumn[Association["Data" -> {{3, {0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10}, ".........."}, {}, None}, "ElementType" -> "String"]], TabularColumn[Association["Data" -> {{3, {0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10}, ".........."}, {}, None}, "ElementType" -> "String"]], TabularColumn[Association["Data" -> {{2, {0, 408, 693, 1022, 1324, 1626, 1987, 2342, 2697, 3057, 3409}, "ALLELEID=426703;CLNDISDB=MONDO:MONDO:0007295,MedGen:C0376532,Orphanet:1945;CLNDN=Self-limited_epilepsy_with_centrotemporal_spikes;CLNHGVS=NC_000021.9:g.6116503C>T;CLNREVSTAT=no_assertion_criteria_provided;CLNSIG=Pathogenic;CLNSIGSCV=SCV000588340;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;CLNVI=ClinGen:CA409758639;GENEINFO=LOC102724428:102724428;MC=SO:0001583|missense_variant;ORIGIN=1;RS=1555841977ALLELEID=3513480;CLNDISDB=.;CLNDN=U2AF1L5-related_condition;CLNHGVS=NC_000021.9:g.6493127dup;CLNREVSTAT=no_assertion_criteria_provided;CLNSIG=Likely_benign;CLNSIGSCV=SCV005357018;CLNVC=Duplication;CLNVCSO=SO:1000035;GENEINFO=LOC102724594:102724594;MC=SO:0001627|intron_variant;ORIGIN=1ALLELEID=3517719;CLNDISDB=.;CLNDN=CRYAA2-related_condition;CLNHGVS=NC_000021.9:g.6562008C>T;CLNREVSTAT=no_assertion_criteria_provided;CLNSIG=Likely_benign;CLNSIGSCV=SCV005366212;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=LOC102724652:102724652;MC=SO:0001623|5_prime_UTR_variant,SO:0001627|intron_variant;ORIGIN=1ALLELEID=3512086;CLNDISDB=.;CLNDN=CRYAA2-related_condition;CLNHGVS=NC_000021.9:g.6562236C>T;CLNREVSTAT=no_assertion_criteria_provided;CLNSIG=Likely_benign;CLNSIGSCV=SCV005353629;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=LOC102724652:102724652;MC=SO:0001819|synonymous_variant;ORIGIN=1ALLELEID=3515616;CLNDISDB=.;CLNDN=KCNE1B-related_condition;CLNHGVS=NC_000021.9:g.7819485G>A;CLNREVSTAT=no_assertion_criteria_provided;CLNSIG=Likely_benign;CLNSIGSCV=SCV005361104;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=LOC102723475:102723475;MC=SO:0001819|synonymous_variant;ORIGIN=1ALLELEID=728830;CLNDISDB=MedGen:C3661900;CLNDN=not_provided;CLNHGVS=NC_000021.9:g.10541121G>T;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Likely_benign;CLNSIGSCV=SCV001029524;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;CLNVI=ClinGen:CA511479263;GENEINFO=TPTE:7179;MC=SO:0001627|intron_variant,SO:0001819|synonymous_variant;ORIGIN=1;RS=374325784ALLELEID=2324965;CLNDISDB=MedGen:CN169374;CLNDN=not_specified;CLNHGVS=NC_000021.9:g.10541137G>C;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Uncertain_significance;CLNSIGSCV=SCV003666233;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;CLNVI=ClinGen:CA9978559;GENEINFO=TPTE:7179;MC=SO:0001583|missense_variant,SO:0001627|intron_variant;ORIGIN=1ALLELEID=2353142;CLNDISDB=MedGen:CN169374;CLNDN=not_specified;CLNHGVS=NC_000021.9:g.10552695C>G;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Uncertain_significance;CLNSIGSCV=SCV003696803;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;CLNVI=ClinGen:CA9978341;GENEINFO=TPTE:7179;MC=SO:0001583|missense_variant,SO:0001627|intron_variant;ORIGIN=1ALLELEID=2195091;CLNDISDB=MedGen:CN169374;CLNDN=not_specified;CLNHGVS=NC_000021.9:g.10561044T>C;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Uncertain_significance;CLNSIGSCV=SCV003538496;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;CLNVI=ClinGen:CA9978234;GENEINFO=TPTE:7179;MC=SO:0001583|missense_variant,SO:0001623|5_prime_UTR_variant;ORIGIN=1AF_ESP=0.00600;AF_TGP=0.00300;ALLELEID=780215;CLNDISDB=MedGen:C3661900;CLNDN=not_provided;CLNHGVS=NC_000021.9:g.10561201A>G;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Benign;CLNSIGSCV=SCV001122497;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;CLNVI=ClinGen:CA9978176;GENEINFO=TPTE:7179;MC=SO:0001627|intron_variant;ORIGIN=1;RS=201619647"}, {}, None}, "ElementType" -> "String"]]}}]|>|>]