| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132935925-132936181 | Common:2; Rare:42 | ||||
| chr8:132936902-132937197 | Common:1; Rare:48 | ||||
| chr8:132938178-132938638 | Common:3; Rare:83 | ||||
| chr8:132941281-132941631 | Common:6; Rare:94; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr8:132943848-132944055 | Common:1; Rare:32 | ||||
| chr8:132944663-132945198 | Common:3; Rare:99 | ||||
| chr8:132945270-132945495 | Common:1; Rare:34 | ||||
| chr8:132946650-132946947 | Common:4; Rare:45 | ||||
| chr8:132946952-132947138 | Rare:33 | ||||
| chr8:132948423-132948472 | Rare:10 | ||||
| chr8:132948757-132949130 | Common:9; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:132950917-132950942 | Rare:5 | ||||
| chr8:132953621-132954170 | Common:8; Rare:89 | ||||
| chr8:132955117-132955381 | Common:2; Rare:58 | ||||
| chr8:132961794-132962389 | Common:3; Rare:104 |