chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97368899373688994TC23GENIChomozygous117376414
97368925073689251GA32GENIChomozygous117376415
97369241873692419GA29GENIChomozygous117559140
97369868373698684TC40GENIChomozygous117376418
97369890473698905GA28GENIChomozygous117376419
97369957373699574GA41GENICheterozygous117376420
97370121173701212GA23GENICheterozygous117376432
97370425473704255GT23GENICpossibly homozygous117376434
97369987573699876GA11GENICpossibly homozygous117878088
97369989073699891CT8GENIChomozygous117878090