chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104531894245318943G-19GENIChomozygous51442209
104531905145319052A-22GENIChomozygous51442210
104531948845319489CG16GENIChomozygous51873363
104532031145320312TTATGG15GENIChomozygous51873366
104532169545321696TC29GENIChomozygous51873369
104532171145321712AC26GENIChomozygous51873372
104532252245322523AG26GENIChomozygous51873375
104532417045324171TTACTC19GENIChomozygous51442213
104532433945324340AG22GENIChomozygous52317949
104532434745324348AG21GENIChomozygous52317951
104532436045324362CA--14GENIChomozygous51873381
104532450845324509CT14GENIChomozygous51873384
104532507245325075GGT---21GENIChomozygous51442216
104532664345326644A-29GENIChomozygous51873387
104532723045327231AG25GENIChomozygous51873390
104532913945329140CT22GENIChomozygous51442220
104533007745330078CT20GENIChomozygous51873396
104533054345330544A-7GENICheterozygous51442221
104533058445330592CACACTCT--------2GENIChomozygous52496641
104532263945322644TTTTT-----3GENICheterozygous52496637
104532736445327372AAAAAAAA--------8GENICpossibly homozygous52496639
104533061845330619CCTGT4GENIChomozygous51873399
104533139645331397AC16GENIChomozygous51873402
104533251745332518GGAAAA8GENICheterozygous52372930
104533362745333628GGTAGCTAGC28GENIChomozygous51442227