chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123210480123210481GT22GENIChomozygous111692078
3123210509123210510AG36GENIChomozygous111692079
3123210663123210664AT6GENIChomozygous111692080
3123211679123211680TC25GENIChomozygous111692081
3123212764123212765CT13GENIChomozygous111692082
3123213093123213094GA8GENIChomozygous111692083
3123213309123213310CT9GENIChomozygous111692084
3123213588123213589TA19GENIChomozygous111692085
3123214018123214019TG22GENIChomozygous111692086
3123214646123214647CT23GENIChomozygous111692087
3123215525123215526AT24GENIChomozygous111692088
3123215919123215920AG13GENIChomozygous111692089
3123216926123216927GA14GENIChomozygous111692090
3123217142123217143AG13GENIChomozygous111692091
3123217390123217391CT19GENIChomozygous111692092
3123217471123217472GA20GENIChomozygous111692093
3123219865123219866CT14GENIChomozygous111692094