chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064446910644470GA20GENIChomozygous46279896
191064520210645203TA25GENIChomozygous46279897
191064528010645281GA27GENIChomozygous46279898
191064604110646042CG33GENIChomozygous46279899
191064621610646217TC19GENIChomozygous46059633
191064631410646315T-20GENIChomozygous46279900
191064673710646738TC23GENIChomozygous46059639
191064674510646746TA22GENIChomozygous46059640
191064718310647189GGGGGG------26GENIChomozygous46397431
191064719410647202GGGTGGGA--------28GENIChomozygous46059642
191064740510647406TTC16GENIChomozygous46059643
191064782310647824CT29GENIChomozygous46279901
191064820510648206TG16INTERGENIChomozygous46059646
191064832110648322AAC6INTERGENIChomozygous46232784
191064837910648380GC17INTERGENIChomozygous46059648
191064941810649419GGAACAACAAC10INTERGENICheterozygous46397433
191064941810649419GGAACAACAACAAC10INTERGENICpossibly homozygous46519526
191065019110650192AT26INTERGENIChomozygous46279902
191065046210650463TTCTC19INTERGENICpossibly homozygous46279903
191065067210650673CCT20INTERGENICpossibly homozygous46279904
191065129610651297AC23INTERGENIChomozygous46059650
191065199110651992TTCTTC4INTERGENIChomozygous46397436
191065216110652162AG22INTERGENIChomozygous46279907
191065453910654540GA12INTERGENICpossibly homozygous46279908