| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151020542-151020738 | Common:1; Rare:58 | ||||
| chr5:151027206-151027474 | Common:1; Rare:45 | ||||
| chr5:151080879-151081170 | Common:1; Rare:87 | ||||
| chr5:151157701-151157907 | Common:1; Rare:49 | ||||
| chr5:154038871-154039010 | Common:1; Rare:49 | ||||
| chr5:154445810-154445864 | Rare:18 | ||||
| chr5:154754997-154755314 | Common:4; Rare:94 | ||||
| chr5:154793668-154793964 | Common:1; Rare:115 | ||||
| chr5:154835032-154835213 | Rare:30 | ||||
| chr5:154850568-154850768 | Common:1; Rare:35 | ||||
| chr5:154857779-154857889 | Rare:31 | ||||
| chr5:154858058-154858267 | Common:6; Rare:68 | ||||
| chr5:154858446-154858762 | Common:1; Rare:103 | ||||
| chr5:154938129-154938323 | Common:1; Rare:70 | ||||
| chr5:157460001-157460346 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):2 |