chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167448235167448236GT45GENIChomozygous57773144
3167448419167448420TC35GENIChomozygous57773145
3167449343167449344AG36GENIChomozygous57773146
3167449534167449535GA29GENIChomozygous57773147
3167450155167450156CCA19GENIChomozygous57773148
3167450210167450211CG17GENIChomozygous57773149
3167450212167450213TC15GENIChomozygous57773150
3167450334167450335GGT7GENICpossibly homozygous57773151
3167450336167450337TTGTG7GENICheterozygous58631320
3167450336167450337TTG7GENICheterozygous58660107
3167451150167451151TTATATAC22GENIChomozygous57773153
3167451486167451488TT--3GENICheterozygous58631321
3167452267167452268CCCA30GENICpossibly homozygous57773157
3167452440167452442GG--32GENIChomozygous57773158
3167455110167455111GA29GENIChomozygous57773159
3167455509167455510TC27GENIChomozygous57773160
3167456264167456265CCA20GENIChomozygous57773161