chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064446910644470GA23GENIChomozygous46279896
191064520210645203TA34GENIChomozygous46279897
191064528010645281GA41GENIChomozygous46279898
191064604110646042CG38GENIChomozygous46279899
191064621610646217TC23GENIChomozygous46059633
191064631410646315T-24GENICpossibly homozygous46279900
191064673710646738TC24GENIChomozygous46059639
191064674510646746TA22GENIChomozygous46059640
191064719410647202GGGTGGGA--------39GENIChomozygous46059642
191064740510647406TTC29GENIChomozygous46059643
191064782310647824CT24GENIChomozygous46279901
191064820510648206TG36INTERGENIChomozygous46059646
191064832110648322AAC7INTERGENICheterozygous46232784
191064837910648380GC18INTERGENIChomozygous46059648
191065019110650192AT32INTERGENIChomozygous46279902
191065046210650463TTCTC33INTERGENIChomozygous46279903
191065067210650673CCT26INTERGENICpossibly homozygous46279904
191065129610651297AC35INTERGENIChomozygous46059650
191065216110652162AG24INTERGENIChomozygous46279907
191065453910654540GA24INTERGENIChomozygous46279908
191064718310647189GGGGGG------32GENIChomozygous46397431
191064941810649419GGAACAACAAC12INTERGENIChomozygous46397433
191065199110651992TTCTTC4INTERGENICheterozygous46397436