chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104024774740247748GC42GENIChomozygous781452417
104024797540247976AC57GENIChomozygous781452418
104024828740248288AG46GENICpossibly homozygous781452419
104024830040248301CT47GENIChomozygous781452420
104024957940249580GA66GENIChomozygous781452421
104024970040249701TC48GENIChomozygous781452422
104025008240250083AT69GENIChomozygous781452423
104025400740254008CT74GENICpossibly homozygous781452424