chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199844870199844871GT6GENIChomozygous108502200
1199844871199844872GC6GENIChomozygous108502202
1199844879199844880GA6GENIChomozygous108502204
1199844898199844899GT6GENIChomozygous108502206
1199844913199844914G6GENIChomozygous127472996
1199844915199844916GA7GENIChomozygous121160432
1199844917199844924GGGGGTG7GENIChomozygous127472997
1199844925199844925TTCATAT7GENIChomozygous127472998
1199844950199844951G10GENIChomozygous127472999
1199844954199844954C10GENIChomozygous127473000
1199844966199844967G10GENIChomozygous127473001
1199844969199844970GC11GENIChomozygous108502208
1199844995199844996GC9GENIChomozygous108502216
1199844971199844972GT11GENIChomozygous108502210
1199844973199844974GT11GENIChomozygous108502212
1199844993199844994GT9GENIChomozygous108502214
1199845034199845035GT17GENIChomozygous108502218
1199845040199845041C16GENIChomozygous127473002
1199845046199845046T16GENIChomozygous127473003
1199845047199845048GT17GENIChomozygous120912619
1199845077199845078AG20GENIChomozygous120892471
1199845078199845079GA20GENIChomozygous120475422
1199845058199845059GT19GENIChomozygous120475419
1199845059199845060TG19GENIChomozygous120475420
1199845061199845062TC20GENIChomozygous120475421
1199859405199859406G8GENIChomozygous127473005
1199859411199859412G6GENIChomozygous127473006
1199859415199859416G6GENIChomozygous127473007
1199859417199859418GA6GENIChomozygous121160446
1199859420199859422GG6GENIChomozygous127473008
1199859426199859427GA5GENIChomozygous121160448
1199859432199859435GAG4GENIChomozygous127473009
1199859438199859441GAG4GENIChomozygous127473010
1199859455199859457CG3GENIChomozygous127473012