chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161029368810293689TC12GENIChomozygous111722685
161029390810293909CT31GENIChomozygous112400300
161029413510294136GT8GENICheterozygous125733091
161029413610294137GT9GENICheterozygous111722687
161029428710294288TC17GENIChomozygous111722689
161029447410294475TC14GENIChomozygous111722691
161029453110294532GA24GENIChomozygous111722693
161029466410294665CA8GENIChomozygous111722695
161029467610294677CT12GENIChomozygous111722697
161029560410295605AC8GENIChomozygous111722701
161029578610295787CT6GENIChomozygous111722703
161029603210296033TG6GENIChomozygous111722705
161029637610296377CT18GENIChomozygous111722707
161029640610296407GA14GENICheterozygous111722709
161029656610296567GA5GENIChomozygous111722713
161029743710297438CA12GENIChomozygous111722715
161029763510297636CT20GENIChomozygous111722717
161029799210297993GA23GENIChomozygous111722719
161029822110298222GA11GENIChomozygous111722721
161029822710298228AG10GENIChomozygous111722723
161029885610298857TC13GENIChomozygous111722725
161030048310300484GA5GENIChomozygous111722729
161030049510300496CT6GENIChomozygous111722731
161030074910300750GA14GENIChomozygous112400301
161030148410301485CT16GENIChomozygous111722733
161030150410301505CG12GENIChomozygous111722735
161030162510301626CT19GENIChomozygous111722738
161030166210301663AC9GENIChomozygous111722740
161030263310302634TG6GENIChomozygous111722742
161030263410302635TC7GENIChomozygous111722744
161030273710302738AG14GENIChomozygous111722746
161030275010302751AG16GENIChomozygous111722748
161030288910302890CT11GENIChomozygous111722750
161030290110302902TC15GENIChomozygous111722752
161030321010303211GA11GENIChomozygous111722754
161030451710304518TC6GENIChomozygous111722760
161030466810304669CT10GENIChomozygous111722762
161030471710304718CT12GENIChomozygous111722764
161030475910304760TC11GENIChomozygous111722766