chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
164928227249282273TC28GENIChomozygous112060210
164928543849285439TC7GENIChomozygous111810521
164928726949287270CT30GENICpossibly homozygous112060211
164929703949297040CG24GENIChomozygous112060213
164929788049297881CG43GENIChomozygous111980691
164929794949297950GA38GENIChomozygous111810543
164929849849298499CG28GENIChomozygous111980693
164930512649305127GC36GENIChomozygous112060214
164931035649310357AG18GENIChomozygous111810549
164931359349313594GA28GENIChomozygous112060215
164931646349316464TC11GENIChomozygous111810561
164931923349319234CT38GENIChomozygous111810563
164932100149321002TC21GENIChomozygous111980699
164932102849321029CT21GENIChomozygous112060216
164932292949322930CT21GENIChomozygous111980703
164932311449323115GA28GENIChomozygous111980705
164932322249323223AT21GENIChomozygous111810569
164932330549323306CT26GENIChomozygous111810571
164932526949325270TC27GENIChomozygous111810579
164932595049325951AG24GENIChomozygous111810581
164932619749326198TC46GENIChomozygous111810585
164932807849328079TC33GENIChomozygous111810591
164932844049328441AC29GENIChomozygous111810593
164931588149315882GT4GENIChomozygous112374935