Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:98255355-98255476 | Common:1; Rare:42 | ||||
chr9:98255550-98255849 | Common:3; Rare:92 | ||||
chr9:99221916-99222355 | Common:2; Rare:171; Clinvar:2; Clinvar (benign):2 | ||||
chr9:99906597-99906696 | Rare:50 | ||||
chr9:100098951-100099314 | Common:3; Rare:103; Clinvar:2 | ||||
chr9:100352854-100353081 | Rare:82 | ||||
chr9:101398585-101398910 | Common:1; Rare:103 | ||||
chr9:101533748-101533905 | Rare:51 | ||||
chr9:104093985-104094321 | Common:3; Rare:78 | ||||
chr9:104747612-104747776 | Rare:50 | ||||
chr9:108933925-108934510 | Common:9; Rare:231; Clinvar:7; Clinvar (benign):3 | ||||
chr9:110256414-110256684 | Common:2; Rare:97 | ||||
chr9:110579197-110579252 | Rare:17 | ||||
chr9:111661487-111661694 | Common:3; Rare:59 | ||||
chr9:112333596-112333944 | Rare:107 |