| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149129539-149129711 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377600-149377811 | Common:1; Rare:50 | ||||
| chr3:149657952-149658200 | Rare:53 | ||||
| chr3:149813158-149813303 | Common:1; Rare:52 | ||||
| chr3:150603149-150603365 | Common:2; Rare:85 | ||||
| chr3:150703255-150703542 | Rare:60 | ||||
| chr3:152268816-152269189 | Rare:122 | ||||
| chr3:152269200-152269335 | Rare:38 | ||||
| chr3:152269539-152269759 | Common:2; Rare:62 | ||||
| chr3:152269852-152270052 | Common:4; Rare:51 | ||||
| chr3:154121244-154121474 | Common:3; Rare:98 | ||||
| chr3:154324317-154324573 | Rare:101 | ||||
| chr3:155079837-155080201 | Common:1; Rare:83 | ||||
| chr3:155854361-155854763 | Rare:110 | ||||
| chr3:156674364-156674664 | Common:3; Rare:87 |