chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45883874658838747GA12GENIChomozygous112662951
45884110158841102GA15GENIChomozygous112662961
45884567558845676CG7GENICheterozygous113112940
45884602758846028TC20GENIChomozygous126014706
45884505258845053TA13GENIChomozygous113235308
45884322958843230CA22GENIChomozygous113235306
45884328758843288CA12GENIChomozygous113235307
45884829258848293CT14GENIChomozygous113235309
45885019858850199TG12GENIChomozygous112662970
45885080058850801CT21GENIChomozygous113235313
45885112758851128CT13GENIChomozygous113235314
45885400458854005AG9GENIChomozygous112662981
45885502958855030GA5GENIChomozygous113235315
45885589358855894GA4GENIChomozygous113026633
45885590158855902AG4GENIChomozygous113026634
45885691458856915CT17GENIChomozygous113235316
45885701358857014GA20GENIChomozygous113026635
45885728358857284CT17GENIChomozygous113026636
45885737858857379TG9GENIChomozygous113026637
45885743758857438CT16GENIChomozygous113026638
45885798158857982AG15GENICheterozygous113026641
45885856058858561AG18GENIChomozygous113235318
45887718158877182CT6GENICheterozygous126048971
45887802458878025TG7GENIChomozygous126048972
45887833558878336TC9GENIChomozygous126048973
45887891658878917GA13GENIChomozygous126048974
45887905158879052AG14GENIChomozygous126014709
45887907658879077GC13GENIChomozygous126048975
45887912358879124TC9GENIChomozygous126048976
45887925058879251CG12GENIChomozygous126048977
45887931858879319CT18GENIChomozygous126048978
45888051458880515GC7GENIChomozygous126048979
45888140258881403AC11GENIChomozygous126048980
45888406358884064TG19GENIChomozygous126048981
45888571458885715TC10GENIChomozygous126048982
45888587458885875GA5GENIChomozygous126048983
45889035558890356CT12GENIChomozygous126048984