chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393276120393277GA31GENIChomozygous54859820
7120393749120393750TC29GENIChomozygous54084096
7120394682120394683AACAGCTAGAC23GENIChomozygous54084097
7120394797120394798TC27GENIChomozygous54084098
7120394923120394924TC12GENIChomozygous54084099
7120394944120394945TG10GENIChomozygous54084100
7120395441120395442TC33GENIChomozygous54084101
7120395946120395947TTG16GENICpossibly homozygous54084102
7120395961120395962TTTTG16GENICheterozygous54084103
7120395961120395962TTG16GENICpossibly homozygous55001602
7120398835120398836CCGTGTGTGT16INTERGENIChomozygous54084105
7120398935120398936CT31INTERGENIChomozygous54859821
7120399434120399435GA14INTERGENIChomozygous54084106
7120399450120399451AG15INTERGENIChomozygous54084107
7120399540120399541GA21INTERGENIChomozygous54084108
7120399996120399997TA13INTERGENIChomozygous54084110
7120400039120400040TC14INTERGENIChomozygous54084111
7120400336120400337CCTG35INTERGENIChomozygous54084112
7120400502120400503GA25INTERGENIChomozygous54084113
7120400517120400518AG27INTERGENIChomozygous54084114
7120400659120400660CT21INTERGENIChomozygous54084115
7120400735120400736GA25INTERGENICpossibly homozygous54084116
7120400751120400752AT25INTERGENICpossibly homozygous54084117
7120400864120400865CT15INTERGENICpossibly homozygous54084118
7120401158120401159AG35INTERGENIChomozygous54084119
7120402309120402310TC41INTERGENIChomozygous54084120