chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005437210054373AC36INTERGENIChomozygous809167453
141005587110055872GA25INTERGENIChomozygous809167454
141005799910058000TC31INTERGENIChomozygous809167455
141005837210058373AG56INTERGENIChomozygous809167456
141005839310058394AC53INTERGENICpossibly homozygous809167457
141005854510058546CA51INTERGENIChomozygous809167458
141005858910058590CT64INTERGENIChomozygous809167459
141005869510058696CT57INTERGENIChomozygous809167460
141005889610058897GA74INTERGENIChomozygous809167461
141005934910059350GA37INTERGENIChomozygous809167462
141006074310060744CT33GENIChomozygous809167463
141006082010060821AG39GENIChomozygous809167464
141006096610060967CT37GENIChomozygous809167465
141006108710061088GC47GENIChomozygous809167466
141006114010061141CT36GENIChomozygous809167467
141006114210061143AT36GENIChomozygous809167468
141006115310061154TC41GENIChomozygous809167469
141006119810061199GA49GENIChomozygous809167470
141006141410061415AC58GENICpossibly homozygous809167471
141006142010061421GA55GENICpossibly homozygous809167472
141006142310061424TA55GENIChomozygous809167473
141006144610061447CA59GENIChomozygous809167474
141006157910061580AG56GENIChomozygous809167475
141006158510061586AG54GENIChomozygous809167476
141006159510061596GA54GENICpossibly homozygous809167477
141006163110061632CT50GENIChomozygous809167478
141006168610061687TC51GENIChomozygous809167479
141006169310061694AG48GENIChomozygous809167480
141006169410061695AG47GENIChomozygous809167481
141006170010061701CT53GENIChomozygous809167482
141006187310061874GA51GENIChomozygous809167483
141006187510061876CA51GENIChomozygous809167484