chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167448235167448236GT58GENIChomozygous57773144
3167448419167448420TC45GENIChomozygous57773145
3167449343167449344AG53GENICpossibly homozygous57773146
3167449534167449535GA52GENIChomozygous57773147
3167450155167450156CCA41GENIChomozygous57773148
3167450210167450211CG27GENIChomozygous57773149
3167450212167450213TC26GENIChomozygous57773150
3167450334167450335GGT13GENICheterozygous57773151
3167450348167450350TC--15GENIChomozygous57773152
3167451150167451151TTATATAC18GENIChomozygous57773153
3167451486167451487T-2GENIChomozygous57773154
3167451510167451511GT13GENICpossibly homozygous57773155
3167451592167451593C-2GENIChomozygous57773156
3167452267167452268CCCA33GENIChomozygous57773157
3167452440167452442GG--35GENIChomozygous57773158
3167455110167455111GA58GENIChomozygous57773159
3167455509167455510TC39GENICpossibly homozygous57773160
3167456264167456265CCA35GENIChomozygous57773161