chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101582044101582045GA51GENIChomozygous143469183
10101583274101583286GGAGGAGATGGT52GENIChomozygous143436570
10101586476101586477GT33GENIChomozygous143469184
10101586525101586526TC9GENICheterozygous146975857
10101595840101595841GA41GENIChomozygous143469185
10101605927101605928TC32GENIChomozygous143469186
10101617189101617190GT58GENIChomozygous143469187
10101628692101628693TG32GENIChomozygous143469188
10101628698101628699TC32GENIChomozygous143469189
10101635260101635261TC26GENIChomozygous143469190
10101616631101616631GGTACAGGGGTACAGGGGTACAGG9GENIChomozygous146940914
10101633238101633238C11GENIChomozygous144079764
10101635152101635152TATT16GENICpossibly homozygous138702629