chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393749120393750TC23GENIChomozygous54084096
7120394682120394683AACAGCTAGAC20GENIChomozygous54084097
7120394797120394798TC22GENIChomozygous54084098
7120394923120394924TC11GENIChomozygous54084099
7120394944120394945TG9GENIChomozygous54084100
7120395441120395442TC21GENIChomozygous54084101
7120395946120395947TTG15GENICpossibly homozygous54084102
7120395961120395962TTTTG15GENICpossibly homozygous54084103
7120398835120398836CCGTGTGTGTGTGTGTGT3INTERGENIChomozygous55144771
7120399434120399435GA33INTERGENIChomozygous54084106
7120399450120399451AG30INTERGENIChomozygous54084107
7120399540120399541GA27INTERGENIChomozygous54084108
7120399897120399914TGTGGAGTTAAAACAAA-----------------28INTERGENIChomozygous54084109
7120399996120399997TA23INTERGENIChomozygous54084110
7120400039120400040TC26INTERGENIChomozygous54084111
7120400336120400337CCTG20INTERGENIChomozygous54084112
7120400502120400503GA30INTERGENIChomozygous54084113
7120400517120400518AG32INTERGENIChomozygous54084114
7120400659120400660CT21INTERGENIChomozygous54084115
7120400735120400736GA18INTERGENIChomozygous54084116
7120400751120400752AT16INTERGENIChomozygous54084117
7120400864120400865CT31INTERGENIChomozygous54084118
7120401158120401159AG34INTERGENIChomozygous54084119
7120402309120402310TC29INTERGENIChomozygous54084120
7120402715120402716CT28INTERGENIChomozygous54084121