chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119734939119734940CT47GENIChomozygous54082127
7119735737119735738AG37GENIChomozygous54082128
7119737142119737143CT32GENIChomozygous54082129
7119738820119738821GA15GENIChomozygous54082131
7119739193119739194GA29GENIChomozygous54082132
7119740038119740039GGCACACACAGACACACACATGCA35GENIChomozygous55095792
7119740085119740086TC44GENIChomozygous54082133
7119740147119740148CT34GENIChomozygous54082134
7119740157119740158CCAGACACACACAG29GENIChomozygous54920992
7119740189119740190CT32GENIChomozygous54082135
7119740285119740286CCACACACACAG20GENIChomozygous54920994
7119740419119740420CCAT19GENICpossibly homozygous55095794
7119740501119740502GA21GENIChomozygous54082136
7119741030119741031GGT16GENIChomozygous54082138