| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152268398-152268653 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr3:152269845-152270061 | Common:4; Rare:56 | ||||
| chr3:152298980-152299351 | Common:1; Rare:80 | ||||
| chr3:154121229-154121463 | Common:3; Rare:101 | ||||
| chr3:154324321-154324581 | Rare:103 | ||||
| chr3:155854350-155854748 | Rare:109 | ||||
| chr3:155870323-155870727 | Common:2; Rare:118 | ||||
| chr3:156674327-156674669 | Common:4; Rare:101 | ||||
| chr3:156826115-156826307 | Common:3; Rare:57 | ||||
| chr3:157160029-157160324 | Rare:122 | ||||
| chr3:157160699-157160739 | Rare:10 | ||||
| chr3:157543276-157543424 | Rare:33 | ||||
| chr3:158105739-158105864 | Common:5; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158672550-158672892 | Common:4; Rare:82 | ||||
| chr3:158732777-158732944 | Rare:21 |