chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172228099172228100CT17GENIChomozygous579010512
1172228130172228131CT30GENIChomozygous579010513
1172228157172228158AG27GENIChomozygous579010514
1172229335172229336TG22GENICpossibly homozygous579010515
1172229596172229597CCCAT11GENIChomozygous716922762
1172230036172230037CT5GENIChomozygous579010516
1172230042172230043C-6GENIChomozygous716922763
1172230454172230455TC25GENIChomozygous579010517
1172230961172230962AG8GENIChomozygous579010518
1172230972172230973GA2GENIChomozygous579010519
1172231004172231005C-6GENIChomozygous716922764
1172231339172231340GA13GENIChomozygous579010520
1172231528172231529A-4GENIChomozygous716922765
1172231556172231557CCT2GENICheterozygous716922766
1172233269172233270TC19GENIChomozygous579010521
1172234597172234598TC14GENIChomozygous579010522
1172234600172234601AG13GENIChomozygous579010523
1172235064172235065CT16GENICpossibly homozygous579010524
1172235892172235893TC24GENIChomozygous579010525
1172237383172237384AG16GENICpossibly homozygous579010526
1172237548172237549TTGTGTGTGTGA7GENIChomozygous716922767
1172237593172237594AG13GENICheterozygous579010527
1172237694172237695CT8GENIChomozygous579010528
1172238366172238367CT20GENICpossibly homozygous579010529
1172239598172239599AACTCT12GENICheterozygous716922768
1172239939172239940GA22GENIChomozygous579010530
1172240054172240055GGCACCCAAA2GENIChomozygous716922769
1172240055172240056GGGCA3GENIChomozygous716922770
1172240448172240449AG19GENICpossibly homozygous579010531
1172241237172241238CCTT9GENICpossibly homozygous716922771
1172241470172241471GA3GENICheterozygous579010532