chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6146124492146124493CCGTGTGT18GENICheterozygous54766761
6146124492146124493CCGTGTGTGT18GENICheterozygous54766762
6146125754146125757AAA---10GENIChomozygous54766763
6146126397146126398CT19GENIChomozygous54766764
6146127571146127572CT20GENIChomozygous54766765
6146127830146127840GCGTGTGTGA----------12GENIChomozygous54766766
6146128730146128731CA27GENIChomozygous54766769
6146130058146130059AG22GENIChomozygous54766770
6146130280146130281CT22GENIChomozygous54766771
6146127868146127876GTGTGTGT--------8GENICheterozygous55547289
6146127870146127876GTGTGT------8GENICpossibly homozygous55547291