chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2246542768246542769AG12GENIChomozygous59484973
2246542994246542995CT14GENICpossibly homozygous59484975
2246543975246543976TC14GENICpossibly homozygous59484977
2246545190246545191TC1GENIChomozygous59484985
2246545194246545195TC1GENIChomozygous59484987
2246551775246551776AT9GENIChomozygous59484997
2246553450246553451TTA1GENIChomozygous59485000
2246554704246554705CT19GENICpossibly homozygous59485002
2246555077246555078AG9GENICpossibly homozygous59485004
2246555620246555621CT9GENIChomozygous59485006
2246556569246556570CA17GENIChomozygous59485008
2246557169246557170TA10GENICpossibly homozygous59485010
2246557199246557200AG11GENICheterozygous59485011
2246557542246557543TA10GENIChomozygous59485013
2246558309246558310TG6GENICheterozygous59485017
2246558744246558745GC15GENIChomozygous59485019
2246558775246558776CT15GENIChomozygous59485021
2246558866246558867CT21GENICheterozygous59485023
2246559968246559969GA18GENIChomozygous59485025
2246560250246560251AAC9GENIChomozygous59485029
2246560883246560884T-7GENIChomozygous59485031
2246560890246560891GT7GENIChomozygous59485033
2246561007246561008GA21GENIChomozygous59485035
2246563107246563108AG14GENIChomozygous59485046
2246563162246563170AAACAAAC--------3GENICheterozygous59485048
2246563471246563472TC28GENICpossibly homozygous59485050
2246563750246563751CT23GENIChomozygous59485052
2246564432246564433CT14GENICpossibly homozygous59485054
2246564642246564643GC13GENICpossibly homozygous59485056
2246567081246567082TTA8GENIChomozygous59485058
2246565921246565922CT6GENICheterozygous60463097