chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393749120393750TC49GENIChomozygous54084096
7120394682120394683AACAGCTAGAC22GENIChomozygous54084097
7120394797120394798TC21GENICpossibly homozygous54084098
7120394923120394924TC18GENIChomozygous54084099
7120394944120394945TG16GENIChomozygous54084100
7120395441120395442TC35GENIChomozygous54084101
7120395940120395952TTTTTTTTTTTT------------14GENICpossibly homozygous54234173
7120396585120396586TTC4GENICheterozygous54234175
7120397351120397358TTTTTTT-------8INTERGENICheterozygous54234177
7120398547120398548CT50INTERGENIChomozygous54234179
7120398835120398836CCGTGTGTGT9INTERGENIChomozygous54084105
7120399450120399451AG56INTERGENIChomozygous54084107
7120400025120400026CT55INTERGENIChomozygous54234181
7120400039120400040TC58INTERGENICpossibly homozygous54084111
7120400336120400337CCTG52INTERGENIChomozygous54084112
7120401121120401122GA47INTERGENICpossibly homozygous54234183
7120401158120401159AG50INTERGENIChomozygous54084119
7120401985120401986GT41INTERGENICpossibly homozygous54234185
7120402236120402237TC54INTERGENIChomozygous54234187
7120402309120402310TC41INTERGENICpossibly homozygous54084120
7120403066120403067CG32INTERGENIChomozygous54234189