chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2069564276956429AC--10GENICheterozygous45776077
2069565516956552AG13GENIChomozygous45754682
2069566036956604GA20GENICpossibly homozygous45776078
2069567406956741CT19GENICpossibly homozygous45754684
2069569826956983AC2GENICheterozygous45406651
2069572776957278GT22GENICpossibly homozygous45754686
2069574246957425CT11GENIChomozygous45754690
2069577136957714GC14GENICpossibly homozygous45406658
2069603256960326GA4GENIChomozygous45776080
2069604156960416CT14GENIChomozygous45754697
2069605596960560AG9GENICpossibly homozygous45406660
2069605696960570GC8GENICpossibly homozygous45754701
2069605876960588AC13GENIChomozygous45754703
2069607266960727GGGC8GENIChomozygous45776081
2069610996961100CG11GENICheterozygous45754709
2069611126961113GA8GENICheterozygous45776082
2069611286961129CG7GENIChomozygous45754711
2069613836961384CT14GENIChomozygous45754715
2069615426961543CT19GENIChomozygous45754716
2069616736961674AG10GENIChomozygous45754720
2069616996961701TG--2GENIChomozygous45621701
2069617046961705TG1GENIChomozygous45818868
2069618566961857TTA2GENIChomozygous45406668
2069618846961885GT2GENIChomozygous45754726
2069618956961896CT1GENIChomozygous45754728
2069618966961897AG1GENIChomozygous45754729