chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167448235167448236GT30GENIChomozygous57773144
3167448419167448420TC14GENIChomozygous57773145
3167449343167449344AG26GENIChomozygous57773146
3167449534167449535GA23GENIChomozygous57773147
3167450155167450156CCA24GENIChomozygous57773148
3167450210167450211CG16GENIChomozygous57773149
3167450212167450213TC16GENIChomozygous57773150
3167450334167450335GGT5GENIChomozygous57773151
3167450336167450337TTGTG2GENICheterozygous58631320
3167451150167451151TTATATAC21GENIChomozygous57773153
3167451486167451488TT--9GENICheterozygous58631321
3167452267167452268CCCA19GENICpossibly homozygous57773157
3167452440167452442GG--15GENIChomozygous57773158
3167455110167455111GA20GENIChomozygous57773159
3167455509167455510TC16GENIChomozygous57773160
3167456264167456265CCA15GENIChomozygous57773161