chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393749120393750TC31GENIChomozygous54084096
7120394682120394683AACAGCTAGAC20GENIChomozygous54084097
7120394797120394798TC21GENIChomozygous54084098
7120394923120394924TC17GENIChomozygous54084099
7120394944120394945TG11GENIChomozygous54084100
7120395441120395442TC20GENIChomozygous54084101
7120395940120395952TTTTTTTTTTTT------------15GENIChomozygous54234173
7120396585120396586TTC12GENICpossibly homozygous54234175
7120397351120397358TTTTTTT-------6INTERGENIChomozygous54234177
7120398547120398548CT29INTERGENIChomozygous54234179
7120398835120398836CCGTGTGTGTGTGTGTGTGT3INTERGENIChomozygous55096047
7120399450120399451AG35INTERGENIChomozygous54084107
7120400025120400026CT33INTERGENIChomozygous54234181
7120400039120400040TC36INTERGENIChomozygous54084111
7120400336120400337CCTG29INTERGENIChomozygous54084112
7120401121120401122GA32INTERGENIChomozygous54234183
7120401158120401159AG29INTERGENIChomozygous54084119
7120401985120401986GT34INTERGENIChomozygous54234185
7120402236120402237TC21INTERGENICpossibly homozygous54234187
7120402309120402310TC34INTERGENICpossibly homozygous54084120
7120403066120403067CG36INTERGENIChomozygous54234189