| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152268805-152269332 | Rare:169 | ||||
| chr3:152269545-152269677 | Rare:35 | ||||
| chr3:152835026-152835197 | Common:2; Rare:58 | ||||
| chr3:154121290-154121463 | Common:3; Rare:79 | ||||
| chr3:154324412-154324571 | Rare:62 | ||||
| chr3:155854364-155854815 | Rare:130 | ||||
| chr3:155870323-155870760 | Common:2; Rare:121 | ||||
| chr3:156553652-156554086 | Common:3; Rare:98 | ||||
| chr3:156554958-156555335 | Common:1; Rare:151 | ||||
| chr3:156674333-156674659 | Common:4; Rare:99 | ||||
| chr3:156826158-156826359 | Common:3; Rare:67 | ||||
| chr3:157160027-157160334 | Rare:124 | ||||
| chr3:158105732-158105898 | Common:5; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158109836-158110204 | Rare:85 | ||||
| chr3:158110313-158110463 | Common:1; Rare:41 |