| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:141531925-141532165 | Rare:40 | ||||
| chr8:142314551-142314835 | Common:2; Rare:69 | ||||
| chr8:142353325-142353566 | Common:1; Rare:50 | ||||
| chr8:142806162-142806194 | Rare:2 | ||||
| chr8:143252403-143252710 | Common:1; Rare:76 | ||||
| chr8:143281616-143281739 | Common:3; Rare:36 | ||||
| chr8:143317796-143317973 | Common:3; Rare:68 | ||||
| chr8:143739210-143739434 | Common:2; Rare:49 | ||||
| chr8:143804787-143805087 | Common:1; Rare:133 | ||||
| chr8:143812710-143812850 | Common:2; Rare:64 | ||||
| chr8:143816757-143817012 | Common:1; Rare:80 | ||||
| chr8:143850447-143850560 | Common:2; Rare:25 | ||||
| chr8:143876811-143876851 | Common:1; Rare:6 | ||||
| chr8:143888381-143888521 | Rare:27 | ||||
| chr8:143925784-143925988 | Common:2; Rare:87; Clinvar:7; Clinvar (benign):6 |