chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393749120393750TC12GENIChomozygous54084096
7120394682120394683AACAGCTAGAC22GENIChomozygous54084097
7120394797120394798TC8GENIChomozygous54084098
7120394923120394924TC7GENIChomozygous54084099
7120394944120394945TG6GENIChomozygous54084100
7120395441120395442TC6GENIChomozygous54084101
7120395938120395939GGGTTTTTTT6GENICheterozygous55030408
7120395946120395947TTG7GENICheterozygous54084102
7120395961120395962TTTTG6GENICheterozygous54084103
7120398835120398836CCGTGTGTGTGTGTGTGT2INTERGENIChomozygous55144771
7120399434120399435GA15INTERGENIChomozygous54084106
7120399450120399451AG15INTERGENIChomozygous54084107
7120399540120399541GA19INTERGENIChomozygous54084108
7120399897120399914TGTGGAGTTAAAACAAA-----------------12INTERGENIChomozygous54084109
7120399996120399997TA15INTERGENIChomozygous54084110
7120400039120400040TC15INTERGENIChomozygous54084111
7120400336120400337CCTG13INTERGENIChomozygous54084112
7120400502120400503GA25INTERGENIChomozygous54084113
7120400517120400518AG29INTERGENIChomozygous54084114
7120400659120400660CT21INTERGENIChomozygous54084115
7120400735120400736GA12INTERGENIChomozygous54084116
7120400751120400752AT14INTERGENIChomozygous54084117
7120400864120400865CT19INTERGENIChomozygous54084118
7120401158120401159AG20INTERGENIChomozygous54084119
7120402309120402310TC32INTERGENIChomozygous54084120
7120402715120402716CT27INTERGENIChomozygous54084121