chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34311073343110734AG2GENIChomozygous58124114
34311161643111617CT8GENIChomozygous59674519
34311197243111973GT12GENICpossibly homozygous58124118
34311258543112586AG20GENICpossibly homozygous58124120
34311297843112979CT14GENIChomozygous58124121
34311307343113074TA21GENICpossibly homozygous58124122
34311327143113272TC12GENICpossibly homozygous58124123
34311328443113285GT10GENICpossibly homozygous58124124
34311331143113312AC13GENIChomozygous58124125
34311352343113524TC15GENIChomozygous58124126
34311373343113734CG3GENIChomozygous58124128
34311417043114171TC20GENICpossibly homozygous58124129
34311494143114956AGTTAACAAAATCAA---------------4GENICheterozygous58124131
34311533643115337GA16GENICpossibly homozygous58124133
34311547343115474GA24GENICpossibly homozygous58124134
34311552343115524TC13GENICpossibly homozygous58124135
34311593643115937GT1GENIChomozygous58124136
34311592943115930AC2GENIChomozygous58736475
34311593243115933CA1GENIChomozygous58736477