chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005815610058157TA15GENICheterozygous973709555
141005815810058159TA21GENIChomozygous973709556
141005837210058373AG11GENIChomozygous973709557
141005839310058394AC15GENIChomozygous973709558
141005854510058546CA15GENIChomozygous973709559
141005889610058897GA26GENIChomozygous973709560
141006082010060821AG23GENIChomozygous973709561
141006091510060916TA16GENIChomozygous973709562
141006096610060967CT23GENIChomozygous973709563
141006108710061088GC19GENIChomozygous973709564
141006114010061141CT16GENIChomozygous973709565
141006114210061143AT16GENIChomozygous973709566
141006115310061154TC16GENIChomozygous973709567
141006119810061199GA17GENIChomozygous973709568
141006129410061295GT6GENIChomozygous973709569
141006133910061340TG17GENIChomozygous973709570
141006141410061415AC26GENIChomozygous973709571
141006142010061421GA26GENIChomozygous973709572
141006142310061424TA25GENIChomozygous973709573
141006144610061447CA22GENIChomozygous973709574
141006157910061580AG15GENIChomozygous973709575
141006158510061586AG14GENIChomozygous973709576
141006159510061596GA13GENIChomozygous973709577
141006163110061632CT17GENIChomozygous973709578
141006168610061687TC21GENIChomozygous973709579
141006169310061694AG20GENIChomozygous973709580
141006169410061695AG20GENIChomozygous973709581
141006170010061701CT19GENIChomozygous973709582
141006187310061874GA17GENIChomozygous973709583
141006187510061876CA18GENIChomozygous973709584