| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129160911-129161520 | Common:29; Rare:190 | ||||
| chr3:129161639-129161840 | Common:1; Rare:49 | ||||
| chr3:129183561-129183684 | Rare:47 | ||||
| chr3:129183687-129184182 | Common:4; Rare:179 | ||||
| chr3:129249470-129249726 | Common:3; Rare:73 | ||||
| chr3:129278734-129278845 | Common:1; Rare:36 | ||||
| chr3:129316192-129316350 | Rare:75 | ||||
| chr3:129439489-129439612 | Rare:29 | ||||
| chr3:129439745-129440484 | Common:5; Rare:230; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129440532-129440581 | Rare:10 | ||||
| chr3:129893326-129893944 | Common:2; Rare:215 | ||||
| chr3:130093752-130093947 | Common:1; Rare:37 | ||||
| chr3:130094235-130094357 | Rare:31 | ||||
| chr3:130746724-130747054 | Common:3; Rare:86 | ||||
| chr3:130850371-130850663 | Rare:47 |