chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144162408144162409TA47GENIChomozygous114152213
5144163972144163973CT44GENIChomozygous114036704
5144164283144164284CT46GENICpossibly homozygous114152214
5144166396144166397TA49GENICpossibly homozygous114152215
5144166417144166418GT50GENIChomozygous114036705
5144166860144166861GA53GENIChomozygous114152216
5144167565144167566TC62GENIChomozygous114036706
5144168918144168919GA52GENIChomozygous114152217
5144169140144169141GA64GENIChomozygous114152218
5144169302144169303TC46GENIChomozygous114152219
5144169921144169922TC52GENIChomozygous114036707
5144169938144169939AG54GENIChomozygous114036708
5144170286144170287CA42GENIChomozygous114152220
5144170288144170289CA42GENIChomozygous114152221
5144170628144170629GA61GENICpossibly homozygous114152222
5144171171144171172AG57GENIChomozygous114036709
5144172390144172391CT49GENICpossibly homozygous114152223
5144173684144173685CA50GENICpossibly homozygous114152224
5144174710144174711TC32GENICpossibly homozygous114036711
5144175012144175013GA42GENICpossibly homozygous114152225
5144175239144175240GT64GENIChomozygous114036712
5144176574144176575CA56GENIChomozygous114152226
5144176990144176991GC53GENIChomozygous114152227
5144177478144177479CG57GENIChomozygous114152228