chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1104147922104147923GA8GENICpossibly homozygous121039621
1104148247104148248AT34GENIChomozygous108904619
1104148454104148455GT31GENIChomozygous121039624
1104148456104148457GT31GENIChomozygous121039625
1104148458104148459GT30GENIChomozygous121039626
1104148629104148630TC22GENIChomozygous109119016
1104152862104152863CT27GENIChomozygous109119018
1104150562104150563AC10GENIChomozygous127546316
1104150568104150569TC7GENIChomozygous127546317
1104150570104150571TC7GENIChomozygous127546318
1104153703104153704AG27GENIChomozygous108904635
1104154420104154421CT31GENIChomozygous109119020
1104154504104154505GA28GENIChomozygous109119022
1104155182104155183TG21GENIChomozygous109119032
1104154661104154662TG33GENICpossibly homozygous109119024
1104154998104154999AG26GENIChomozygous109119026
1104155081104155082GA16GENIChomozygous109119028
1104155162104155163CT21GENIChomozygous109119030
1104155975104155976GA27GENIChomozygous109119034
1104160128104160129AG31GENIChomozygous109119036
1104163398104163399TC29GENIChomozygous108904649
1104163519104163520GC27GENIChomozygous109119038
1104165108104165109TC29GENIChomozygous109119040
1104161854104161854GACA14GENIChomozygous130818933
1104162867104162867CTG31GENIChomozygous130818934