chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243820926243820927GA39GENIChomozygous110349753
2243823686243823687CT61GENIChomozygous110349755
2243821978243821978TTG56GENICpossibly homozygous127757243
2243822653243822653TTGTTCA53GENIChomozygous127757244
2243827856243827856A39GENIChomozygous127757245
2243827933243827934CT48GENIChomozygous110349757
2243828744243828745CT40GENIChomozygous110349759
2243828827243828828GA35GENIChomozygous110349761
2243830136243830137AG33GENIChomozygous110349763
2243830546243830547TA31GENIChomozygous110349765
2243831374243831375GA40GENIChomozygous110349767
2243831469243831470AC42GENIChomozygous110349769
2243831715243831716AG49GENIChomozygous110349771
2243832865243832865G56GENIChomozygous127757246
2243832882243832883AG52GENIChomozygous110349773
2243833698243833698GAGT24GENICheterozygous127757247
2243835983243835984TC47GENIChomozygous110349779
2243838420243838421AG38GENIChomozygous110349783
2243838424243838425AG37GENIChomozygous110349785
2243838428243838429AG39GENIChomozygous110349786
2243838686243838687GA54GENIChomozygous110349788
2243838872243838873GA59GENIChomozygous110349790
2243839763243839764GC45GENICpossibly homozygous110349792
2243840407243840408T49GENIChomozygous127757248
2243840592243840593TA48GENIChomozygous110349794
2243841888243841889GC41GENIChomozygous110349796
2243842892243842893CA39GENIChomozygous110349798
2243843349243843350TC44GENIChomozygous110349800
2243843452243843453AG35GENIChomozygous110349802
2243844178243844179AC45GENIChomozygous110349804
2243846103243846104CA67GENIChomozygous110349806
2243847663243847664GT42GENIChomozygous110349808
2243847969243847970CA39GENIChomozygous110349810
2243848359243848360CT54GENIChomozygous110349812
2243849051243849052GA48GENIChomozygous110349814
2243849732243849733AG27GENIChomozygous120131791
2243850179243850180GA44GENIChomozygous110349816
2243852504243852505GA38GENIChomozygous110349818