chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45761162157611622AC15GENIChomozygous56908643
45761560257615604AA--2GENIChomozygous57321966
45761597357615974A-1GENIChomozygous57321968
45761840557618406CT20GENICpossibly homozygous57321970
45762229457622295CT10GENICheterozygous56908669
45762345257623453CCT1GENIChomozygous56908675
45762509357625094TC19GENIChomozygous57321980
45762511757625118CT19GENICpossibly homozygous56908685
45762524057625241CT25GENIChomozygous57321982
45762581557625816AG17GENICpossibly homozygous56908688
45762684257626843AATG11GENICpossibly homozygous56908692
45762699757626998TA7GENIChomozygous57321984
45762699857626999CT7GENIChomozygous57321986
45762786257627863AT15GENIChomozygous57321988
45762872957628730T-10GENIChomozygous56908695
45762915157629152AG16GENIChomozygous56908696
45762958557629586CT8GENIChomozygous56908697
45762998257629983TC17GENIChomozygous56908698
45763007757630078TC21GENICpossibly homozygous56908699
45763035657630357GA14GENIChomozygous57321992
45763087857630879GA4GENIChomozygous56908703
45763089957630900GA5GENIChomozygous56908704
45763201957632020G-7GENIChomozygous57321994
45763303057633031GA18GENICpossibly homozygous57321996
45763322457633225TG14GENIChomozygous56908706
45763339657633397GA9GENICheterozygous57321998
45763376957633770TC13GENICheterozygous57322000
45763413257634133AG25GENIChomozygous56908709
45763532057635322TT--2GENICheterozygous57322002
45763702757637028AG2GENIChomozygous56908731
45763789957637900AG22GENIChomozygous56908737
45762594357625944AAAC1GENIChomozygous58279360
45763531757635318CCTT2GENICheterozygous58279362