| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149475678-149475898 | Common:2; Rare:76 | ||||
| chr3:150408087-150408364 | Common:2; Rare:102 | ||||
| chr3:150410864-150410988 | Rare:48 | ||||
| chr3:150603151-150603398 | Common:2; Rare:100 | ||||
| chr3:150763458-150763610 | Rare:38 | ||||
| chr3:152268555-152269169 | Common:2; Rare:223 | ||||
| chr3:152269190-152269347 | Rare:46 | ||||
| chr3:152269559-152269696 | Rare:36 | ||||
| chr3:154121262-154121457 | Common:3; Rare:84 | ||||
| chr3:155853927-155853989 | Rare:18 | ||||
| chr3:155854074-155854109 | Rare:6 | ||||
| chr3:155854322-155854815 | Common:1; Rare:135; Clinvar (benign):1 | ||||
| chr3:155870323-155870763 | Common:2; Rare:122 | ||||
| chr3:156674353-156674656 | Common:3; Rare:91 | ||||
| chr3:156826182-156826311 | Common:2; Rare:43 |