chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1244683104244683105GT15GENICpossibly homozygous120846634
1244686863244686864AC30GENIChomozygous108596099
1244712837244712839GA14GENIChomozygous127499600
1244712848244712849AG13GENIChomozygous108596112
1244720577244720578AC55GENICheterozygous121205500
1244756735244756736TC39GENIChomozygous108596114
1244720583244720583T50GENICheterozygous130217990