chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39125357991253580AG25GENIChomozygous119980144
39125394791253947T14GENIChomozygous127908488
39125431491254315T13GENIChomozygous127908489
39125532591255326GA14GENIChomozygous119980145
39125577891255779AG16GENIChomozygous111653725
39125615291256153AG11GENIChomozygous119980146
39125428791254287T13GENICheterozygous131625917
39125509391255094C27GENIChomozygous131625918
39125515591255157AG19GENIChomozygous131625919
39125605291256052GC14GENICheterozygous131625920
39125542291255423AT12GENIChomozygous120018039
39125601091256011GA20GENIChomozygous131637086
39125621391256238CTTTCTTTCTTTCTTTCTTTCTTTC11GENIChomozygous131625921
39125626791256268AG10GENIChomozygous111653726
39125790691257907AC18GENIChomozygous111653727
39125816791258168TC9GENIChomozygous119980147
39125845691258457TC20GENIChomozygous111653728
39125882691258827TA9GENIChomozygous111653729
39125965191259652GA24GENIChomozygous119980148
39126017891260179TC16GENIChomozygous111653732
39126030891260309GA11GENIChomozygous112253790
39126150291261503GA28GENIChomozygous111653733
39126169891261699AC14GENIChomozygous111653734
39126251391262514GA12GENIChomozygous131637087
39126263791262638TC6GENIChomozygous111653736
39126367191263672GA27GENIChomozygous119980149
39126408191264082A19GENIChomozygous127908491
39126472991264730T11GENIChomozygous131625922
39126642691266427AT6GENIChomozygous131637088
39126665691266656AAC12GENICheterozygous131625923
39126668091266681CA13GENIChomozygous111653740
39126710091267101GA21GENIChomozygous111653742
39126718891267189TC24GENIChomozygous112253794
39126796991267969T24GENICpossibly homozygous131625924
39126829691268296GGTT19GENIChomozygous131625925
39126852991268529TGC19GENIChomozygous131625926
39126866891268669AG28GENIChomozygous112253795
39126888591268886GA17GENIChomozygous119980150
39126941291269413TG21GENIChomozygous112253796
39126978891269794CCTGGT21GENIChomozygous131625927
39127081191270812AC26GENIChomozygous111653746