| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:90001392-90001542 | Rare:70 | ||||
| chr8:90645002-90645148 | Rare:41 | ||||
| chr8:90645590-90645880 | Common:4; Rare:105 | ||||
| chr8:90646036-90646220 | Common:4; Rare:48 | ||||
| chr8:90646380-90646750 | Common:2; Rare:88 | ||||
| chr8:90985209-90985387 | Common:3; Rare:54 | ||||
| chr8:91040539-91041104 | Common:3; Rare:166 | ||||
| chr8:91070020-91070364 | Common:1; Rare:124 | ||||
| chr8:92965530-92965776 | Common:2; Rare:66 | ||||
| chr8:92966131-92966292 | Common:1; Rare:43 | ||||
| chr8:93700458-93700650 | Common:1; Rare:76 | ||||
| chr8:93740931-93741232 | Common:1; Rare:100 | ||||
| chr8:93754717-93754965 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):5 | ||||
| chr8:93916588-93916968 | Common:7; Rare:131; Clinvar (benign):1 | ||||
| chr8:93917680-93917904 | Common:1; Rare:78 |