| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123396353-123396569 | Common:2; Rare:98 | ||||
| chr8:124538981-124539198 | Common:2; Rare:126; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091725-125091914 | Common:2; Rare:66; Clinvar (benign):3 | ||||
| chr8:133571854-133572163 | Rare:74 | ||||
| chr8:141001142-141001459 | Common:2; Rare:113 | ||||
| chr8:142777821-142777938 | Rare:23 | ||||
| chr8:143018409-143018575 | Common:1; Rare:46 | ||||
| chr8:143541430-143541658 | Common:2; Rare:75 | ||||
| chr8:143558236-143558387 | Common:1; Rare:49 | ||||
| chr8:143617464-143617759 | Common:2; Rare:111 | ||||
| chr8:143635893-143636058 | Common:2; Rare:72 | ||||
| chr8:143684369-143684502 | Common:3; Rare:27 | ||||
| chr8:143939512-143939789 | Common:4; Rare:80 | ||||
| chr8:144078553-144078722 | Common:1; Rare:50 | ||||
| chr8:144082494-144082677 | Common:2; Rare:63 |