| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152835016-152835128 | Common:1; Rare:42 | ||||
| chr3:154121261-154121457 | Common:3; Rare:84 | ||||
| chr3:154324412-154324584 | Rare:67 | ||||
| chr3:155079830-155080019 | Common:1; Rare:48 | ||||
| chr3:155080146-155080407 | Common:1; Rare:68 | ||||
| chr3:155854350-155854811 | Rare:131 | ||||
| chr3:155870356-155870783 | Common:2; Rare:118 | ||||
| chr3:156456873-156457093 | Common:2; Rare:38 | ||||
| chr3:156554992-156555428 | Common:2; Rare:162 | ||||
| chr3:156674343-156674653 | Common:4; Rare:92 | ||||
| chr3:156826066-156826323 | Common:3; Rare:67 | ||||
| chr3:157159905-157160344 | Common:1; Rare:176 | ||||
| chr3:157381601-157381983 | Common:3; Rare:69 | ||||
| chr3:158105726-158105902 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:158106236-158106274 | Rare:10 |