chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85324792053247921CT24GENIChomozygous116820338
85324834453248345TG31GENIChomozygous116820340
85324847853248479AG26GENIChomozygous116820342
85324862353248624TC22GENIChomozygous116820344
85324876853248769GA27GENIChomozygous116820346
85324892853248929TC24GENIChomozygous116820348
85324911153249112GA24GENIChomozygous116820350
85324916953249170GA20GENIChomozygous116820352
85324920353249204GA11GENICheterozygous116820354
85324925053249251GT17GENICheterozygous116820358
85324948653249487AC14GENIChomozygous116820360
85324952353249524TG12GENIChomozygous116820362
85324959653249597CT22GENIChomozygous116820364
85325062453250625AG18GENIChomozygous116820366
85325154353251544CG11GENIChomozygous116820372
85326406453264065GA24GENIChomozygous116820374
85326411053264111CT4GENIChomozygous116820376
85327052253270523GA10GENIChomozygous116820378
85327388253273883TC15GENIChomozygous116820380
85327395753273958AC24GENIChomozygous116820382
85327501953275020AG13GENIChomozygous116820384
85327522253275223AT6GENICheterozygous126685436
85327532753275328GA20GENICheterozygous116820386
85327658553276586AG17GENIChomozygous116820388
85327788253277883GT8GENIChomozygous116820394