chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157512057157512067GGCACTGGAG51GENIChomozygous136925213
4157512459157512461AC47GENIChomozygous136925214
4157512473157512475AC46GENICpossibly homozygous136925215
4157512758157512765ATTAACA51GENIChomozygous136925216
4157512775157512776AG54GENIChomozygous137248595
4157514037157514038CG58GENIChomozygous137248596
4157514226157514227TC29GENIChomozygous137248597
4157514631157514632GA46GENIChomozygous137248598
4157517341157517342GA60GENIChomozygous137248599
4157514183157514184GC29GENICheterozygous403125148
4157514183157514184G29GENICpossibly homozygous403125147