chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167448235167448236GT39GENIChomozygous57773144
3167448419167448420TC23GENIChomozygous57773145
3167449343167449344AG33GENIChomozygous57773146
3167449534167449535GA27GENIChomozygous57773147
3167450155167450156CCA22GENIChomozygous57773148
3167450334167450335GGT22GENICheterozygous57773151
3167450348167450350TC--23GENICpossibly homozygous57773152
3167451150167451151TTATATAC13GENIChomozygous57773153
3167451486167451487T-2GENIChomozygous57773154
3167451510167451511GT15GENIChomozygous57773155
3167451592167451593C-1GENIChomozygous57773156
3167451664167451665C-2GENIChomozygous58246515
3167452267167452268CCCA20GENICpossibly homozygous57773157
3167452440167452442GG--26GENIChomozygous57773158
3167455110167455111GA47GENIChomozygous57773159
3167455509167455510TC33GENIChomozygous57773160
3167456264167456265CCA16GENIChomozygous57773161