chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39786635397866354AT20GENIChomozygous57571068
39786636497866365TA18GENIChomozygous57571070
39786663597866636CT18GENIChomozygous60018973
39786700697867007CA27GENICpossibly homozygous60018974
39786741597867416CT24GENIChomozygous60018975
39786750897867509AG25GENICpossibly homozygous57571074
39786779697867797A-21GENIChomozygous60018976
39786786597867866GA26GENIChomozygous57571078
39786792897867929TC15GENIChomozygous57571080
39786802097868021TC21GENIChomozygous57571082
39786829497868295AG16GENIChomozygous60018977
39786860597868606CCA28GENIChomozygous60018978
39786868097868681AC21GENIChomozygous57571088
39786878297868783TA28GENIChomozygous60018979
39786917197869172CT13GENIChomozygous60018980
39786921197869212AG20GENIChomozygous57571092
39786927497869275TTG26GENIChomozygous57571094
39786960497869605CT30GENIChomozygous57571096
39786980297869803CT34GENIChomozygous57571098
39787059797870598TG29GENIChomozygous57571100
39787147897871479GC23GENIChomozygous57571104
39787267797872678CA25GENIChomozygous57571106
39787273297872733TC29GENIChomozygous57571108
39787290697872907GA30GENIChomozygous60018981
39787300197873002AG19GENIChomozygous57571110
39787307297873073CT26GENIChomozygous57571112
39787388597873886TC27GENIChomozygous57571114
39787417497874175AC35GENIChomozygous57571116
39787418597874186AC40GENIChomozygous57571118
39787486897874869AT19GENIChomozygous60018982
39787499397874994GA30GENIChomozygous57571120
39787674297876746GTTA----26GENIChomozygous57571122