| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149752428-149752544 | Common:2; Rare:44 | ||||
| chr3:149812708-149812768 | Rare:19 | ||||
| chr3:150408692-150408988 | Rare:96 | ||||
| chr3:150603151-150603367 | Common:2; Rare:86 | ||||
| chr3:150703261-150703542 | Rare:58 | ||||
| chr3:150703702-150704018 | Common:3; Rare:162 | ||||
| chr3:152268540-152269192 | Common:2; Rare:230 | ||||
| chr3:152269196-152269335 | Rare:39 | ||||
| chr3:152269509-152269749 | Common:2; Rare:71 | ||||
| chr3:152834940-152835152 | Common:2; Rare:65 | ||||
| chr3:154121303-154121474 | Common:3; Rare:77 | ||||
| chr3:154324312-154324573 | Rare:102 | ||||
| chr3:155079837-155080166 | Common:1; Rare:76 | ||||
| chr3:155080171-155080384 | Common:1; Rare:50 | ||||
| chr3:155854292-155854817 | Common:1; Rare:140; Clinvar (benign):1 |