chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119077573690775737TC43GENIChomozygous50864457
119077692290776923CA59GENIChomozygous50864458
119077713590777136TG52GENICpossibly homozygous50864459
119077713690777137TC52GENIChomozygous50864460
119077897290778973AC53GENICpossibly homozygous50864461
119077901190779012AG58GENIChomozygous50864462
119077938090779381AG52GENIChomozygous50864463
119078227690782277GA34GENIChomozygous50864464
119078237390782374G-41GENIChomozygous50864465
119078247090782471G-44GENIChomozygous50864466
119078251890782519CT49GENIChomozygous50864467
119078252890782529CA43GENIChomozygous50864468
119078257990782580AAGTGTGTGT4GENIChomozygous50864469
119078281290782813TA41GENICheterozygous50864470
119078283490782835GC39GENICheterozygous50864471
119078319390783196TTT---10GENICpossibly homozygous50864472
119078320590783206GA14GENICheterozygous50864473
119078322190783222TTTA9GENICheterozygous50864474
119078324190783242CA8GENICpossibly homozygous50864475
119078327290783273AAT9GENIChomozygous50864476
119078327790783278AAG14GENICheterozygous50864477
119078329390783295GC--11GENIChomozygous50864478
119078330290783303GA17GENIChomozygous50864479
119078370790783708TG57GENIChomozygous50864480
119078437890784379AG43GENIChomozygous50864481
119078461590784616AG31GENIChomozygous50864482
119078582390785824TC35GENICpossibly homozygous50864483