chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172227740172227741TC17GENICheterozygous510427345
1172227750172227770GCCTTGCGCTCGCTAGGCAA--------------------11GENICheterozygous685131032
1172228099172228100CT46GENIChomozygous507172624
1172228130172228131CT48GENIChomozygous507172625
1172228157172228158AG46GENIChomozygous507172626
1172229335172229336TG56GENIChomozygous507172627
1172229596172229597CCCAT42GENIChomozygous685131033
1172230036172230037CT27GENICpossibly homozygous507172628
1172230042172230043C-24GENIChomozygous685131034
1172230454172230455TC62GENIChomozygous507172629
1172230961172230962AG52GENIChomozygous507172630
1172230972172230973GA52GENIChomozygous507172631
1172231004172231005C-59GENIChomozygous685131035
1172231339172231340GA53GENIChomozygous507172632
1172231528172231529A-37GENIChomozygous685131036
1172231556172231557CCT19GENIChomozygous685131037
1172231621172231622TTA4GENIChomozygous685131038
1172233269172233270TC64GENICpossibly homozygous507172633
1172234597172234598TC41GENIChomozygous507172634
1172234600172234601AG41GENIChomozygous507172635
1172234989172234991AG--17GENICheterozygous685131039
1172234994172234995GT13GENICheterozygous510427346
1172234995172234997AC--5GENICheterozygous685131040
1172235006172235007CT24GENICheterozygous510427347
1172235064172235065CT44GENIChomozygous507172636
1172235892172235893TC64GENIChomozygous507172637
1172237383172237384AG53GENICpossibly homozygous507172638
1172237547172237549GT--32GENICheterozygous685131041
1172237567172237568AG40GENICheterozygous510427348
1172237593172237594AG50GENICpossibly homozygous507172639
1172237693172237695GC--55GENICheterozygous685131042
1172238366172238367CT66GENIChomozygous507172640
1172239598172239599AACTCT44GENIChomozygous685131043
1172239939172239940GA60GENIChomozygous507172641
1172240054172240055GGCACCCAAA28GENIChomozygous685131044
1172240055172240056GGGCA20GENIChomozygous685131045
1172240448172240449AG57GENIChomozygous507172642
1172241470172241471GA55GENIChomozygous507172643