chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172228157172228158AG12GENIChomozygous668336968
1172229335172229336TG12GENICpossibly homozygous668336969
1172229596172229597CCCAT19GENIChomozygous768111889
1172230036172230037CT7GENICpossibly homozygous668336970
1172230042172230043C-9GENICpossibly homozygous768111890
1172230118172230119AG20GENIChomozygous668336971
1172230454172230455TC13GENICpossibly homozygous668336972
1172230961172230962AG4GENIChomozygous668336973
1172230972172230973GA1GENIChomozygous668336974
1172231004172231005C-1GENIChomozygous768111891
1172231298172231299GA16GENIChomozygous668336975
1172231339172231340GA9GENICpossibly homozygous668336976
1172231528172231529A-11GENICpossibly homozygous768111892
1172232328172232329CT18GENIChomozygous668336977
1172233269172233270TC13GENIChomozygous668336978
1172234321172234322GT14GENICheterozygous668336979
1172234597172234598TC7GENIChomozygous668336980
1172234600172234601AG8GENIChomozygous668336981
1172235064172235065CT13GENIChomozygous668336982
1172235249172235250CT7GENIChomozygous668336983
1172235254172235255AG8GENIChomozygous668336984
1172235892172235893TC24GENIChomozygous668336985
1172237383172237384AG6GENICheterozygous668336986
1172237548172237549TTGTGTGTGTGA2GENIChomozygous768111893
1172237593172237594AG13GENIChomozygous668336987
1172237694172237695CT3GENICheterozygous668336988
1172238366172238367CT16GENICpossibly homozygous668336989
1172239598172239599AACTCT6GENICheterozygous768111895
1172239939172239940GA9GENIChomozygous668336990
1172240448172240449AG8GENICheterozygous668336991
1172240515172240516CT16GENIChomozygous668336992
1172241237172241238CCTT5GENIChomozygous768111896
1172241411172241412CT8GENIChomozygous668336993
1172241470172241471GA5GENICheterozygous668336994