chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1235893958235893959AG55GENIChomozygous144573027
1235893975235893976GA57GENIChomozygous144573028
1235894241235894242GA58GENIChomozygous146356583
1235895036235895036AG45GENIChomozygous135466966
1235895216235895217AC57GENIChomozygous144573030
1235895546235895547CT57GENIChomozygous146356584
1235895709235895710AG55GENIChomozygous144573031
1235895890235895891AC53GENIChomozygous146356585
1235896060235896061CT43GENIChomozygous146356586
1235896492235896493AC61GENIChomozygous144573032
1235897080235897081GA44GENIChomozygous144573033
1235897141235897142CT50GENICpossibly homozygous146356587
1235897319235897321AT50GENIChomozygous144529855
1235897352235897353AG49GENIChomozygous144573034
1235898197235898198AG66GENIChomozygous144573037
1235898207235898208GA64GENIChomozygous146356588
1235898342235898343AC46GENIChomozygous144573038
1235898453235898454CT46GENIChomozygous144573039
1235899085235899085G50GENIChomozygous144529856
1235900022235900023GT42GENIChomozygous142874736
1235897575235897576TC43GENIChomozygous135838676
1235898869235898870TC62GENIChomozygous135838678
1235899252235899253AG57GENIChomozygous135838679
1235897630235897630A44GENIChomozygous146336760
1235900734235900735TC44GENIChomozygous142874737
1235900983235900984AG34GENIChomozygous142874738
1235901310235901311CG42GENIChomozygous146356589