chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10102302979102302980CA5GENIChomozygous116958840
10102302982102302983CA5GENIChomozygous116832444
10102366395102366396CT11GENIChomozygous116832454
10102366411102366412GC7GENIChomozygous116832456
10102366412102366413CA7GENIChomozygous116832458
10102366678102366679GA13GENIChomozygous116958848
10102367130102367131CT8GENIChomozygous117089051
10102367111102367112GA10GENIChomozygous117089045
10102367123102367124TC8GENIChomozygous117089047
10102367126102367127CT7GENIChomozygous117089049
10102372325102372326GC14GENICheterozygous117089053
10102403604102403605TG9GENICheterozygous117089055
10102445432102445433TC13GENICheterozygous117089057
10102456044102456045TG10GENIChomozygous116713431
10102456045102456046GT10GENIChomozygous116713433
10102490537102490538TC4GENIChomozygous116713489
10102490539102490540GC4GENIChomozygous116713491
10102490541102490542AC4GENIChomozygous116713493
10102560771102560772TG25GENIChomozygous116713499
10102561043102561044TG12GENIChomozygous117089059