chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225036286225036287CT17INTERGENICpossibly homozygous61926307
1225036343225036344GC23INTERGENIChomozygous61100956
1225036638225036639CT8INTERGENIChomozygous61100957
1225037306225037307AG9INTERGENICpossibly homozygous61100958
1225037336225037337AC10INTERGENIChomozygous61100959
1225038014225038018CCCC----1INTERGENIChomozygous61100960
1225038568225038569CT10INTERGENICpossibly homozygous61100962
1225040131225040132GC11INTERGENIChomozygous61100963
1225040759225040760CT11INTERGENIChomozygous61926309
1225042365225042366CT15INTERGENICpossibly homozygous61926310
1225042457225042458AG1INTERGENIChomozygous61926311
1225042461225042462AG1INTERGENIChomozygous61926312
1225042465225042466AG2INTERGENICheterozygous61926313
1225043136225043137CT24INTERGENICpossibly homozygous61926314
1225044196225044197TC12INTERGENIChomozygous61100966
1225044326225044327CT21INTERGENIChomozygous61100967
1225044396225044397CT12INTERGENICheterozygous61100968
1225044427225044428AAGT12INTERGENICpossibly homozygous61100969
1225044476225044477CT19INTERGENICpossibly homozygous61926315
1225045520225045521AC17INTERGENICheterozygous61100971
1225045832225045833CT11INTERGENICheterozygous61926316