chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160019163160019164CT24GENIChomozygous111791166
3160019897160019898AT22GENIChomozygous111791168
3160020509160020510GA33GENICpossibly homozygous111791170
3160021913160021914CT12GENIChomozygous111791172
3160021928160021929CA11GENIChomozygous111791173
3160025195160025196CT21GENIChomozygous111791179
3160027220160027221GA37GENIChomozygous111791181
3160028426160028427CT29GENICpossibly homozygous111791183
3160029828160029829AG27GENIChomozygous111791185
3160030498160030499TC35GENIChomozygous111791187
3160033762160033763TC33GENIChomozygous111791189
3160035292160035293AT19GENIChomozygous111791191
3160035465160035466TC29GENIChomozygous111791193
3160035634160035635GA30GENIChomozygous111791195
3160036519160036520AG24GENIChomozygous111791197
3160036697160036698TC22GENIChomozygous111791199
3160036713160036714GA24GENIChomozygous111791201