| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:35640035-35640113 | Rare:25 | ||||
| chr3:35640122-35640168 | Rare:13 | ||||
| chr3:35641515-35641643 | Common:3; Rare:15 | ||||
| chr3:36992415-36992744 | Common:1; Rare:100 | ||||
| chr3:36993056-36993563 | Common:2; Rare:173; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993727-36993840 | Rare:45 | ||||
| chr3:37176233-37176393 | Rare:52 | ||||
| chr3:37243146-37243365 | Common:1; Rare:59 | ||||
| chr3:37861989-37862184 | Rare:56 | ||||
| chr3:38164968-38165279 | Common:1; Rare:77 | ||||
| chr3:38165429-38165849 | Common:1; Rare:142 | ||||
| chr3:38496735-38496793 | Rare:12 | ||||
| chr3:39051924-39052085 | Common:1; Rare:58 | ||||
| chr3:39052361-39052548 | Common:1; Rare:61 | ||||
| chr3:39107539-39107741 | Common:4; Rare:62 |