chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1235893958235893959AG61GENIChomozygous144573027
1235893975235893976GA57GENIChomozygous144573028
1235894161235894162GA51GENIChomozygous144573029
1235894771235894771G58GENIChomozygous144529854
1235895036235895036AG49GENIChomozygous135466966
1235895216235895217AC41GENICpossibly homozygous144573030
1235895709235895710AG46GENIChomozygous144573031
1235896492235896493AC47GENIChomozygous144573032
1235897080235897081GA44GENIChomozygous144573033
1235897319235897321AT63GENIChomozygous144529855
1235897352235897353AG66GENIChomozygous144573034
1235897371235897372CT60GENIChomozygous144573035
1235897546235897547CT33GENIChomozygous144573036
1235898197235898198AG64GENIChomozygous144573037
1235898342235898343AC64GENIChomozygous144573038
1235898453235898454CT38GENIChomozygous144573039
1235898869235898870TC58GENIChomozygous135838678
1235897575235897576TC25GENIChomozygous135838676
1235899085235899085G54GENIChomozygous144529856
1235899252235899253AG46GENIChomozygous135838679
1235899901235899902TC49GENIChomozygous144573040
1235900022235900023GT41GENIChomozygous142874736