chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172227802172227803GT10GENIChomozygous825411417
1172228099172228100CT8GENIChomozygous825411418
1172228157172228158AG15GENIChomozygous825411419
1172229335172229336TG9GENIChomozygous825411420
1172230036172230037CT19GENIChomozygous825411421
1172230042172230043C-19GENIChomozygous825411422
1172230093172230094GA16GENICheterozygous825411423
1172230454172230455TC14GENIChomozygous825411424
1172230961172230962AG16GENIChomozygous825411425
1172230972172230973GA14GENIChomozygous825411426
1172231004172231005C-14GENIChomozygous825411427
1172231339172231340GA19GENIChomozygous825411428
1172231528172231529A-12GENIChomozygous825411429
1172231556172231557CCT8GENIChomozygous825411430
1172233065172233074CTCTGTACC---------13GENIChomozygous825411431
1172233075172233076AC13GENIChomozygous825411432
1172233269172233270TC12GENIChomozygous825411433
1172233416172233417CT15GENIChomozygous825411434
1172234597172234598TC17GENIChomozygous825411435
1172234600172234601AG17GENIChomozygous825411436
1172235064172235065CT11GENIChomozygous825411437
1172235109172235110GGC13GENIChomozygous825411438
1172235892172235893TC17GENIChomozygous825411439
1172237383172237384AG13GENIChomozygous825411440
1172237548172237549TTGTGTGTGTGA9GENIChomozygous825411441
1172237593172237594AG10GENIChomozygous825411442
1172237694172237695CT10GENIChomozygous825411443
1172239598172239599AACTCT16GENIChomozygous825411444
1172240054172240055GGCACCCAAA13GENIChomozygous825411445
1172240055172240056GGGCA13GENIChomozygous825411446
1172240448172240449AG7GENIChomozygous825411447
1172240952172240953TC7GENIChomozygous825411448