| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152268397-152269198 | Common:3; Rare:261; Clinvar (benign):1 | ||||
| chr3:152269200-152269357 | Rare:44 | ||||
| chr3:152269444-152269759 | Common:2; Rare:99 | ||||
| chr3:152269845-152270052 | Common:4; Rare:51 | ||||
| chr3:152298941-152299413 | Common:1; Rare:94 | ||||
| chr3:152834931-152835213 | Common:2; Rare:84 | ||||
| chr3:154121262-154121463 | Common:3; Rare:88 | ||||
| chr3:154121496-154121792 | Common:2; Rare:88 | ||||
| chr3:155854364-155854798 | Rare:124 | ||||
| chr3:156674362-156674651 | Common:3; Rare:85 | ||||
| chr3:156826140-156826355 | Common:3; Rare:67 | ||||
| chr3:157159843-157159897 | Rare:11 | ||||
| chr3:157160027-157160334 | Rare:124 | ||||
| chr3:157160697-157160991 | Common:5; Rare:71 | ||||
| chr3:158672560-158672871 | Common:4; Rare:76 |