| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:123036648-123036813 | Common:3; Rare:95 | ||||
| chr5:123423253-123423607 | Common:1; Rare:186 | ||||
| chr5:123511980-123512385 | Common:3; Rare:195 | ||||
| chr5:126472051-126472632 | Common:7; Rare:279 | ||||
| chr5:126595121-126595448 | Common:10; Rare:235; Clinvar:16; Clinvar (benign):22; Clinvar (pathogenic):6 | ||||
| chr5:126600601-126601071 | Common:6; Rare:234 | ||||
| chr5:126776787-126777251 | Common:7; Rare:314; Clinvar:12; Clinvar (benign):12 | ||||
| chr5:127030537-127030766 | Common:4; Rare:104 | ||||
| chr5:127073436-127073544 | Common:4; Rare:35 | ||||
| chr5:127073449-127073561 | Common:3; Rare:37 | ||||
| chr5:127517375-127517768 | Common:13; Rare:264 | ||||
| chr5:128083537-128083768 | Common:4; Rare:162 | ||||
| chr5:129094450-129094762 | Common:6; Rare:240 | ||||
| chr5:129095140-129095460 | Common:2; Rare:146 | ||||
| chr5:129904161-129904592 | Common:4; Rare:191 |