chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
156051838060518381GA18GENIChomozygous558439197
156052210260522103TA4GENIChomozygous558439198
156053698160536982A-2GENICheterozygous704074133
156053711360537114GGA4GENICheterozygous704074137
156053714560537146AAG14GENIChomozygous704074138
156053751060537511CCG23GENIChomozygous704074139
156055147360551474CCA2GENIChomozygous704074143
156056387360563874A-16GENIChomozygous704074144
156056388160563882AAT15GENIChomozygous704074145
156056389960563900GT20GENIChomozygous558439199
156056390060563901GT20GENIChomozygous558439200
156056396860563969AC17GENIChomozygous558439201
156056396960563970AT17GENIChomozygous558439202
156056397260563973AC18GENIChomozygous558439203
156056397360563974AG18GENIChomozygous558439204
156056397460563975AC18GENIChomozygous558439205
156056486760564868AG21GENIChomozygous556401468
156058174160581743GT--17GENICheterozygous704074146
156059289160592892CCT9GENICheterozygous704074147
156063590260635903CCT3GENICheterozygous704074148
156063699860636999AG15GENIChomozygous556401469
156064203060642032GT--4GENICheterozygous704074151
156064682260646824AC--2GENICheterozygous704074155
156064774360647745GT--9GENICheterozygous704074156
156067603560676037GG--6GENICheterozygous704074157
156067603660676037G-6GENICheterozygous704074158
156067969860679700CA--11GENICheterozygous704074160
156068638560686386TG7GENIChomozygous558439206