chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106743188767431888AG30GENIChomozygous116795557
106743969867439699TC23GENIChomozygous116795559
106744424067444241CT28GENICpossibly homozygous116795561
106744434767444348GT21GENIChomozygous116795563
106744542367445424CA20GENIChomozygous116795565
106744876867448769TA13GENIChomozygous117255963
106744877067448771CG13GENIChomozygous117255965
106746100667461007AC26GENIChomozygous116795567
106746450267464503GA29GENIChomozygous116795569
106746653267466533TC26GENIChomozygous116621154
106746975667469757GA23GENIChomozygous116795571
106747128267471283AG24GENIChomozygous116795573
106747158767471588AG25GENIChomozygous116795575