chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123210480123210481GT27GENIChomozygous111692078
3123210509123210510AG34GENIChomozygous111692079
3123210663123210664AT15GENIChomozygous111692080
3123211679123211680TC29GENIChomozygous111692081
3123212764123212765CT14GENIChomozygous111692082
3123213093123213094GA37GENIChomozygous111692083
3123213309123213310CT42GENIChomozygous111692084
3123213588123213589TA29GENIChomozygous111692085
3123214018123214019TG28GENIChomozygous111692086
3123214646123214647CT21GENIChomozygous111692087
3123215525123215526AT25GENIChomozygous111692088
3123215919123215920AG16GENIChomozygous111692089
3123216926123216927GA26GENIChomozygous111692090
3123217142123217143AG13GENIChomozygous111692091
3123217390123217391CT34GENIChomozygous111692092
3123217471123217472GA32GENIChomozygous111692093
3123219865123219866CT19GENIChomozygous111692094
3123220928123220929AG34GENICheterozygous112256138