| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132294243-132294456 | Common:1; Rare:47 | ||||
| chr5:132295150-132295680 | Common:3; Rare:143 | ||||
| chr5:132369150-132369480 | Common:5; Rare:82 | ||||
| chr5:132369488-132370110 | Common:20; Rare:368; Clinvar:18; Clinvar (benign):15; Clinvar (pathogenic):17 | ||||
| chr5:132410603-132410980 | Common:2; Rare:127 | ||||
| chr5:132411000-132411350 | Common:4; Rare:135 | ||||
| chr5:132490761-132491020 | Rare:133 | ||||
| chr5:132556860-132557277 | Rare:209; Clinvar:2 | ||||
| chr5:132737475-132737743 | Rare:137 | ||||
| chr5:132777333-132777479 | Rare:41 | ||||
| chr5:132830550-132830794 | Rare:122 | ||||
| chr5:132830810-132831160 | Common:2; Rare:164 | ||||
| chr5:132866435-132866690 | Common:2; Rare:153; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:132963256-132963424 | Common:1; Rare:59 | ||||
| chr5:132963486-132963825 | Common:1; Rare:158 |