| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17246589-17247108 | Common:5; Rare:209 | ||||
| chr8:17801080-17801344 | Common:7; Rare:99 | ||||
| chr8:17922613-17922944 | Common:4; Rare:124 | ||||
| chr8:17922953-17923018 | Common:1; Rare:30 | ||||
| chr8:17923220-17923328 | Rare:35 | ||||
| chr8:18084820-18085028 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr8:19013629-19013961 | Common:5; Rare:98 | ||||
| chr8:19817345-19817515 | Common:4; Rare:69 | ||||
| chr8:21919509-21919773 | Common:2; Rare:108 | ||||
| chr8:22231975-22232053 | Rare:14 | ||||
| chr8:22232057-22232111 | Rare:18 | ||||
| chr8:22245024-22245499 | Common:2; Rare:172 | ||||
| chr8:22367030-22367331 | Common:6; Rare:98 | ||||
| chr8:22412200-22412335 | Rare:29 | ||||
| chr8:22440980-22441295 | Common:5; Rare:79 |