chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39125357991253580AG59GENIChomozygous119980144
39125394791253947T55GENIChomozygous127908488
39125428791254287T50GENIChomozygous131625917
39125431491254315T47GENIChomozygous127908489
39125509391255094C47GENIChomozygous131625918
39125515591255157AG43GENIChomozygous131625919
39125532591255326GA48GENIChomozygous119980145
39125542291255423AT48GENIChomozygous120018039
39125577891255779AG58GENIChomozygous111653725
39125605291256052GC27GENICheterozygous131625920
39125615291256153AG29GENIChomozygous119980146
39125621391256238CTTTCTTTCTTTCTTTCTTTCTTTC26GENIChomozygous131625921
39125626791256268AG13GENIChomozygous111653726
39125601091256011GA31GENIChomozygous131637086
39125790691257907AC61GENICpossibly homozygous111653727
39125816791258168TC52GENIChomozygous119980147
39125845691258457TC43GENIChomozygous111653728
39125882691258827TA32GENIChomozygous111653729
39125965191259652GA47GENICpossibly homozygous119980148
39126017891260179TC55GENIChomozygous111653732
39126030891260309GA47GENIChomozygous112253790
39126150291261503GA50GENIChomozygous111653733
39126169891261699AC50GENIChomozygous111653734
39126251391262514GA31GENIChomozygous131637087
39126263791262638TC18GENIChomozygous111653736
39126367191263672GA50GENIChomozygous119980149
39126408191264082A47GENIChomozygous127908491
39126472991264730T25GENIChomozygous131625922
39126642691266427AT19GENIChomozygous131637088
39126665691266656AAC29GENIChomozygous131625923
39126668091266681CA27GENIChomozygous111653740
39126710091267101GA43GENIChomozygous111653742
39126718891267189TC47GENIChomozygous112253794
39126796991267969T52GENICpossibly homozygous131625924
39126829691268296GGTT48GENIChomozygous131625925
39126852991268529TGC42GENIChomozygous131625926
39126866891268669AG42GENIChomozygous112253795
39126888591268886GA44GENIChomozygous119980150
39126941291269413TG59GENIChomozygous112253796
39126978891269794CCTGGT62GENIChomozygous131625927
39127081191270812AC55GENIChomozygous111653746