| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144478240-144478453 | Rare:97 | ||||
| chr8:144508470-144508809 | Common:4; Rare:129 | ||||
| chr8:144508858-144509160 | Rare:179 | ||||
| chr8:144517736-144518050 | Common:2; Rare:198; Clinvar:8; Clinvar (benign):1 | ||||
| chr8:144528912-144529202 | Common:4; Rare:245 | ||||
| chr8:144755200-144755980 | Common:4; Rare:373 | ||||
| chr8:144786726-144786899 | Common:2; Rare:113 | ||||
| chr8:144787172-144787572 | Common:7; Rare:159 | ||||
| chr8:144791963-144792623 | Common:9; Rare:413 | ||||
| chr8:144798660-144799020 | Common:5; Rare:158 | ||||
| chr8:144827201-144827629 | Common:5; Rare:230 | ||||
| chr8:144852967-144853168 | Rare:131 | ||||
| chr8:144853478-144853711 | Common:3; Rare:55 | ||||
| chr8:144901400-144901757 | Common:2; Rare:191 | ||||
| chr8:144950605-144950920 | Common:9; Rare:200 |