| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152269529-152269689 | Rare:45 | ||||
| chr3:152835008-152835128 | Common:1; Rare:45 | ||||
| chr3:154324405-154324573 | Rare:67 | ||||
| chr3:155079616-155079736 | Common:4; Rare:43 | ||||
| chr3:155079836-155080400 | Common:2; Rare:135 | ||||
| chr3:155854350-155854763 | Rare:112 | ||||
| chr3:155870367-155870732 | Common:1; Rare:105 | ||||
| chr3:156456844-156456951 | Common:1; Rare:27 | ||||
| chr3:156553991-156554160 | Common:1; Rare:27 | ||||
| chr3:156554980-156555335 | Common:1; Rare:142 | ||||
| chr3:156674327-156674669 | Common:4; Rare:101 | ||||
| chr3:157160083-157160334 | Rare:103 | ||||
| chr3:157533544-157533701 | Common:4; Rare:25 | ||||
| chr3:158105728-158105902 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:158109836-158110173 | Rare:77 |