| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:108924569-108924804 | Rare:81 | ||||
| chr5:109409144-109410505 | Common:49; Rare:1640 | ||||
| chr5:109689133-109689543 | Common:29; Rare:656 | ||||
| chr5:109689741-109690053 | Common:8; Rare:368 | ||||
| chr5:110726499-110727326 | Common:13; Rare:312 | ||||
| chr5:110738621-110739141 | Common:14; Rare:640; Clinvar (pathogenic):1 | ||||
| chr5:110739194-110739594 | Common:5; Rare:194; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:111073108-111073508 | Common:5; Rare:231 | ||||
| chr5:111092074-111092474 | Common:14; Rare:853; Clinvar:13; Clinvar (benign):26 | ||||
| chr5:111092566-111092966 | Rare:185; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:111511463-111512129 | Common:3; Rare:183 | ||||
| chr5:111512390-111512920 | Common:21; Rare:819 | ||||
| chr5:111512967-111513294 | Common:2; Rare:110 | ||||
| chr5:111756913-111757600 | Common:7; Rare:251 | ||||
| chr5:111757547-111757970 | Common:3; Rare:422 |