chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120645654120645655TC10GENICpossibly homozygous54235024
7120648492120648493TC12GENICheterozygous54084753
7120646947120646948G-2GENICheterozygous54084751
7120648402120648403TG12GENICpossibly homozygous54084752
7120649681120649682GA12GENICheterozygous54235026
7120649968120649969CCAT19GENIChomozygous54084755
7120650286120650287GA16GENICheterozygous54235028
7120651078120651079CT6GENICheterozygous54235030
7120653881120653882GA5GENIChomozygous54235034
7120653941120653942GA14GENICpossibly homozygous54235036
7120654230120654233TTT---5GENIChomozygous54235038
7120654333120654334AT10GENICheterozygous54235040
7120654718120654719GA7GENIChomozygous54235042
7120654723120654724GA8GENICpossibly homozygous54235044
7120655085120655086TTAC3GENICheterozygous54235046
7120659067120659093ACGGGGGGGGGGGCATTTCACAAACC--------------------------2GENIChomozygous54235060
7120659098120659099TTC2GENIChomozygous54084757
7120659140120659141GA11GENIChomozygous54235062
7120659475120659476GA6GENICheterozygous54235064
7120659933120659934CT15GENIChomozygous54235066
7120660610120660613CAT---3GENICheterozygous54235068
7120661585120661586CCG16GENIChomozygous54235070
7120661976120661977CG8GENIChomozygous54235072
7120664860120664861TC13GENICpossibly homozygous54235074