chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005437210054373AC3GENIChomozygous950784348
141005837210058373AG24GENIChomozygous950784349
141005839310058394AC25GENIChomozygous950784350
141005854510058546CA20GENIChomozygous950784351
141005858910058590CT16GENIChomozygous950784352
141005869510058696CT28GENIChomozygous950784353
141005889610058897GA24GENIChomozygous950784354
141005934910059350GA29GENIChomozygous950784355
141006074310060744CT22GENIChomozygous950784356
141006082010060821AG20GENIChomozygous950784357
141006096610060967CT13GENIChomozygous950784358
141006108710061088GC19GENIChomozygous950784359
141006114010061141CT21GENIChomozygous950784360
141006114210061143AT20GENIChomozygous950784361
141006115310061154TC20GENIChomozygous950784362
141006119810061199GA20GENIChomozygous950784363
141006141410061415AC12GENICheterozygous950784364
141006142010061421GA10GENIChomozygous950784365
141006142310061424TA9GENIChomozygous950784366
141006144610061447CA10GENIChomozygous950784367
141006157910061580AG14GENIChomozygous950784368
141006158510061586AG16GENIChomozygous950784369
141006159510061596GA16GENIChomozygous950784370
141006163110061632CT20GENIChomozygous950784371
141006168610061687TC28GENIChomozygous950784372
141006169310061694AG28GENIChomozygous950784373
141006169410061695AG28GENIChomozygous950784374
141006170010061701CT27GENIChomozygous950784375
141006187310061874GA20GENIChomozygous950784376
141006187510061876CA20GENIChomozygous950784377