chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243551211243551212AG14GENIChomozygous110347900
2243551266243551266A13GENIChomozygous127757096
2243551698243551699A20GENIChomozygous127757097
2243551784243551785TC13GENIChomozygous110347902
2243552145243552146A15GENIChomozygous127757098
2243552164243552165TC17GENIChomozygous110347904
2243553059243553060GC28GENIChomozygous110347908
2243553157243553158TG20GENICpossibly homozygous110347910
2243553214243553215AC15GENIChomozygous110347912
2243553319243553320GA22GENIChomozygous110347914
2243553424243553425TC17GENIChomozygous110347916
2243553729243553730AG10GENIChomozygous110347918
2243554499243554500A25GENIChomozygous127757099
2243554515243554517TT25GENIChomozygous127757100
2243554892243554893CG17GENIChomozygous110347920
2243555015243555016AG20GENIChomozygous110347922
2243555276243555277TG15GENIChomozygous110347924
2243556463243556464TA13GENIChomozygous110347955
2243556282243556283TG8GENIChomozygous110633271
2243556902243556903TC19GENIChomozygous110347957
2243557156243557157GA30GENIChomozygous110347959
2243557183243557184TC34GENIChomozygous110347961
2243557344243557345TC22GENIChomozygous110347963
2243557965243557966CT24GENIChomozygous110347965
2243558285243558285T19GENIChomozygous127757101
2243559046243559047GA27GENIChomozygous110347967
2243559064243559073CAGGGTTGT25GENIChomozygous127757102
2243559104243559105CT26GENIChomozygous110347969
2243559231243559232CA21GENIChomozygous110347971
2243559288243559288C19GENIChomozygous127757103
2243559290243559291TG21GENIChomozygous120131779
2243559316243559317AC24GENIChomozygous110347973
2243559682243559683CT25GENIChomozygous110347975
2243559690243559691GA26GENIChomozygous110347977
2243559982243559983CT40GENIChomozygous110347979
2243560178243560179GT25GENIChomozygous110347981
2243560446243560447TG21GENIChomozygous110347983
2243560718243560719AG8GENIChomozygous110347985
2243561110243561111AG21GENIChomozygous110347987
2243561224243561225TC21GENIChomozygous110347989
2243561420243561421AG20GENIChomozygous110347991