chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108897970888979709CA18INTERGENIChomozygous68157653
108897974288979743CG22INTERGENIChomozygous68157657
108898317688983177TG32GENIChomozygous68157660
108898341588983416CA4GENIChomozygous68157663
108898346488983465CT2GENIChomozygous82709039
108898346588983466AC2GENIChomozygous82709040
108898348488983485CG5GENIChomozygous68157666
108898349788983498CA12GENIChomozygous68157669
108898400188984002GC21GENICpossibly homozygous68157691
108898415788984158AG21GENIChomozygous68157694
108898149588981496GA15INTERGENIChomozygous68928912
108898284388982844CT16GENIChomozygous68928914
108898515888985159GC31GENIChomozygous68157715
108898533788985338GA22GENIChomozygous68796752
108898610088986101GA20INTERGENIChomozygous68157728
108898648688986487AG17INTERGENIChomozygous68157730
108898669888986699CA25INTERGENIChomozygous68928916
108898669988986700AT25INTERGENIChomozygous68928918
108898899488988995CT28INTERGENIChomozygous68157733
108898943888989439GC15INTERGENICheterozygous82695759
108898944088989441GC14INTERGENICheterozygous82695761
108899121488991215GA22INTERGENIChomozygous68157736
108899159388991594GA21INTERGENIChomozygous68157739
108899216288992163GT19INTERGENIChomozygous68157742
108899246888992469TG23INTERGENIChomozygous68157745
108899308088993081AG20INTERGENIChomozygous68157748
108899316088993161TC18INTERGENIChomozygous68157751
108899408888994089AC22INTERGENIChomozygous68157754
108899415588994156AG31INTERGENIChomozygous68157757
108899515788995158AG14INTERGENIChomozygous68157763
108899557688995577GT14INTERGENIChomozygous68157765
108899600388996004TC20INTERGENIChomozygous68157768
108899612188996122CA27INTERGENIChomozygous68157771
108899656888996569AG13INTERGENIChomozygous68157774
108899657588996576GA14INTERGENIChomozygous68157777
108899677688996777TC26INTERGENIChomozygous68157781