| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142447968-142448130 | Common:1; Rare:57 | ||||
| chr3:142578690-142578962 | Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:143001429-143001631 | Common:3; Rare:74 | ||||
| chr3:147393364-147393465 | Common:1; Rare:31 | ||||
| chr3:149129549-149129714 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377449-149377875 | Common:1; Rare:116 | ||||
| chr3:150603162-150603447 | Common:3; Rare:120 | ||||
| chr3:152268842-152269053 | Rare:72 | ||||
| chr3:152269540-152269659 | Rare:36 | ||||
| chr3:154324444-154324631 | Rare:60 | ||||
| chr3:155079837-155079995 | Common:1; Rare:41 | ||||
| chr3:155854361-155854752 | Rare:108 | ||||
| chr3:155870323-155870723 | Common:2; Rare:117 | ||||
| chr3:156674364-156674631 | Common:3; Rare:77 | ||||
| chr3:157160090-157160327 | Rare:100 |