chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393749120393750TC30GENIChomozygous54084096
7120394682120394683AACAGCTAGAC25GENIChomozygous54084097
7120394797120394798TC40GENIChomozygous54084098
7120394923120394924TC8GENIChomozygous54084099
7120394944120394945TG5GENIChomozygous54084100
7120395441120395442TC36GENIChomozygous54084101
7120395940120395952TTTTTTTTTTTT------------13GENICheterozygous54234173
7120396585120396586TTC18GENICpossibly homozygous54234175
7120397351120397358TTTTTTT-------3INTERGENICheterozygous54234177
7120398547120398548CT38INTERGENIChomozygous54234179
7120398835120398836CCGTGTGTGTGTGTGTGT2INTERGENIChomozygous55144771
7120399450120399451AG36INTERGENIChomozygous54084107
7120400025120400026CT32INTERGENIChomozygous54234181
7120400039120400040TC24INTERGENIChomozygous54084111
7120400336120400337CCTG27INTERGENIChomozygous54084112
7120401121120401122GA28INTERGENIChomozygous54234183
7120401158120401159AG32INTERGENIChomozygous54084119
7120401985120401986GT35INTERGENIChomozygous54234185
7120402236120402237TC30INTERGENIChomozygous54234187
7120402309120402310TC35INTERGENIChomozygous54084120
7120403066120403067CG25INTERGENIChomozygous54234189