| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:28092787-28093219 | Common:4; Rare:127 | ||||
| chr8:28490214-28490412 | Rare:33 | ||||
| chr8:28494114-28494287 | Common:4; Rare:54 | ||||
| chr8:28622462-28622788 | Common:2; Rare:90 | ||||
| chr8:28701251-28701630 | Common:3; Rare:131 | ||||
| chr8:28889905-28890676 | Rare:210 | ||||
| chr8:29350056-29350518 | Common:2; Rare:129 | ||||
| chr8:29350641-29350925 | Common:2; Rare:71 | ||||
| chr8:30082950-30083318 | Common:2; Rare:110 | ||||
| chr8:30095360-30095507 | Common:1; Rare:46 | ||||
| chr8:30156219-30156406 | Common:1; Rare:61 | ||||
| chr8:30384756-30385064 | Rare:78 | ||||
| chr8:30657978-30658410 | Common:5; Rare:127 | ||||
| chr8:30727563-30727925 | Common:6; Rare:113; Clinvar (benign):1 | ||||
| chr8:30744126-30744424 | Common:3; Rare:101 |