chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34311064943110651AG--2GENIChomozygous60007577
34311073343110734AG25GENIChomozygous58124114
34311144943111450TTACACACAC5GENICheterozygous59098958
34311144943111450TTACACACACACACAC5GENICheterozygous59098960
34311152443111525CCAA15GENIChomozygous59098962
34311197243111973GT17GENIChomozygous58124118
34311214043112141GGAA17GENIChomozygous58124119
34311258543112586AG26GENIChomozygous58124120
34311297843112979CT21GENIChomozygous58124121
34311307343113074TA23GENIChomozygous58124122
34311327143113272TC22GENIChomozygous58124123
34311328443113285GT23GENIChomozygous58124124
34311331143113312AC28GENIChomozygous58124125
34311352343113524TC22GENIChomozygous58124126
34311373343113734CG12GENIChomozygous58124128
34311417043114171TC27GENIChomozygous58124129
34311494143114956AGTTAACAAAATCAA---------------28GENICpossibly homozygous58124131
34311520743115208AAAGGCAGGC26GENIChomozygous59098968
34311533643115337GA20GENIChomozygous58124133
34311547343115474GA30GENIChomozygous58124134
34311552343115524TC31GENICpossibly homozygous58124135
34311593643115937GT9GENICheterozygous58124136
34311593843115939GGCCTGAATTTCAGTCATCCTGTGACGGCCTCCCAGGGGCTGGGGGTACAGC9GENICheterozygous59098974
34311593243115933CA9GENICheterozygous58736477
34311259043112591AG28GENIChomozygous59290607
34311496943114970G-23GENICpossibly homozygous59290610
34311586643115867T-22GENIChomozygous59290612
34311592943115930AC9GENICheterozygous58736475