chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172227750172227770GCCTTGCGCTCGCTAGGCAA--------------------15GENIChomozygous765848469
1172228099172228100CT22GENICpossibly homozygous664530628
1172228130172228131CT17GENIChomozygous664530629
1172228157172228158AG16GENIChomozygous664530630
1172229335172229336TG14GENIChomozygous664530631
1172229596172229597CCCAT21GENICpossibly homozygous765848470
1172230036172230037CT19GENIChomozygous664530632
1172230042172230043C-18GENIChomozygous765848471
1172230454172230455TC20GENIChomozygous664530633
1172230961172230962AG23GENIChomozygous664530634
1172230972172230973GA22GENIChomozygous664530635
1172231004172231005C-16GENIChomozygous765848472
1172231339172231340GA25GENIChomozygous664530636
1172231528172231529A-10GENIChomozygous765848473
1172231556172231557CCT13GENICpossibly homozygous765848474
1172231615172231616TTGAGCTAAATCCCCA1GENIChomozygous765848475
1172233269172233270TC27GENIChomozygous664530637
1172234597172234598TC20GENIChomozygous664530638
1172234600172234601AG19GENIChomozygous664530639
1172234963172235001ACACACAGACAGACACACAGACAGACAGACAGACACAC--------------------------------------7GENIChomozygous765848476
1172235006172235007CT9GENIChomozygous664530640
1172235064172235065CT21GENIChomozygous664530641
1172235892172235893TC23GENIChomozygous664530642
1172237383172237384AG16GENIChomozygous664530643
1172237548172237549TTGTGTGTGTGA25GENIChomozygous765848478
1172237593172237594AG24GENIChomozygous664530644
1172237694172237695CT36GENICpossibly homozygous664530645
1172238366172238367CT23GENIChomozygous664530646
1172239598172239599AACTCT23GENIChomozygous765848479
1172239939172239940GA25GENIChomozygous664530647
1172240054172240055GGCACCCAAA38GENIChomozygous765848480
1172240055172240056GGGCA38GENIChomozygous765848481
1172240448172240449AG18GENIChomozygous664530648
1172241237172241238CCTT10GENIChomozygous765848482
1172241470172241471GA19GENIChomozygous664530649