chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43461493034614931CT18GENICheterozygous57926072
43461506834615069GT16GENICheterozygous57718504
43461708234617083TC15GENIChomozygous56815549
43461781934617820TC15GENIChomozygous57718508
43461803834618039TC18GENIChomozygous57718510
43461871734618718T-17GENICheterozygous56815561
43461913934619140GA11GENIChomozygous57718513
43461947634619477GT21GENIChomozygous56815569
43462030134620302AG15GENIChomozygous56815573
43462032134620322CT12GENIChomozygous57718515
43462048134620482CT13GENIChomozygous57718517
43462070434620705GA12GENIChomozygous57718519
43462070934620710CA12GENIChomozygous57718521
43462073734620738CT15GENIChomozygous56815579
43462114734621148AG15GENIChomozygous57718523
43462115234621155AAA---15GENIChomozygous57718524
43462131434621315GT11GENIChomozygous57718525
43462151934621520GGA11GENIChomozygous56815581
43462184434621846AT--16GENICheterozygous57718526
43462189634621897TC17GENIChomozygous57718527
43462243834622439CT18GENIChomozygous56815589
43462271834622719TTTG12GENIChomozygous56815593
43462276834622769GA13GENIChomozygous56815595
43462291534622916TC12GENIChomozygous56815599
43462308234623083A-11GENIChomozygous56815601
43462309034623091GA11GENIChomozygous56815603
43462356534623566AG12GENIChomozygous56815607
43462403534624036GA10GENIChomozygous56815609
43462423234624233TC14GENIChomozygous56815611
43462055134620552TA11GENIChomozygous58330792