chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225036286225036287CT21INTERGENIChomozygous61926307
1225036343225036344GC23INTERGENIChomozygous61100956
1225036638225036639CT24INTERGENIChomozygous61100957
1225037306225037307AG17INTERGENICheterozygous61100958
1225037336225037337AC14INTERGENIChomozygous61100959
1225038014225038018CCCC----7INTERGENIChomozygous61100960
1225038568225038569CT17INTERGENICpossibly homozygous61100962
1225040131225040132GC18INTERGENIChomozygous61100963
1225040759225040760CT24INTERGENIChomozygous61926309
1225042365225042366CT10INTERGENICpossibly homozygous61926310
1225042465225042466AG1INTERGENIChomozygous61926313
1225043136225043137CT24INTERGENICpossibly homozygous61926314
1225044196225044197TC17INTERGENIChomozygous61100966
1225044326225044327CT22INTERGENIChomozygous61100967
1225044396225044397CT28INTERGENICpossibly homozygous61100968
1225044427225044428AAGT21INTERGENICpossibly homozygous61100969
1225044476225044477CT27INTERGENICpossibly homozygous61926315
1225045520225045521AC16INTERGENICheterozygous61100971
1225045832225045833CT29INTERGENICpossibly homozygous61926316