chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064446910644470GA29GENIChomozygous46279896
191064520210645203TA20GENIChomozygous46279897
191064528010645281GA33GENIChomozygous46279898
191064604110646042CG23GENIChomozygous46279899
191064621610646217TC14GENIChomozygous46059633
191064631410646315T-16GENICpossibly homozygous46279900
191064673710646738TC27GENIChomozygous46059639
191064674510646746TA25GENIChomozygous46059640
191064718310647189GGGGGG------18GENIChomozygous46397431
191064719410647202GGGTGGGA--------19GENIChomozygous46059642
191064740510647406TTC28GENIChomozygous46059643
191064782310647824CT11GENIChomozygous46279901
191064820510648206TG12INTERGENIChomozygous46059646
191064832110648322AAC4INTERGENICheterozygous46232784
191064837910648380GC20INTERGENIChomozygous46059648
191064941810649419GGAACAACAAC6INTERGENIChomozygous46397433
191065019110650192AT21INTERGENIChomozygous46279902
191065046210650463TTCTC34INTERGENIChomozygous46279903
191065067210650673CCT17INTERGENICpossibly homozygous46279904
191065129610651297AC21INTERGENIChomozygous46059650
191065199110651992TTCTTC5INTERGENIChomozygous46397436
191065216110652162AG13INTERGENIChomozygous46279907
191065453910654540GA17INTERGENIChomozygous46279908