| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:154324415-154324573 | Rare:63 | ||||
| chr3:155080077-155080407 | Common:1; Rare:82 | ||||
| chr3:155854373-155854780 | Rare:114 | ||||
| chr3:156674339-156674653 | Common:4; Rare:93 | ||||
| chr3:156826120-156826311 | Common:3; Rare:56 | ||||
| chr3:157160059-157160343 | Rare:116 | ||||
| chr3:157543165-157543473 | Common:2; Rare:67 | ||||
| chr3:158105739-158105902 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158110011-158110162 | Rare:33 | ||||
| chr3:158571064-158571229 | Rare:54 | ||||
| chr3:158732159-158732318 | Common:6; Rare:48 | ||||
| chr3:158801997-158802195 | Common:2; Rare:88 | ||||
| chr3:160399494-160399669 | Rare:46; Clinvar:1 | ||||
| chr3:160565271-160565378 | Common:1; Rare:28 | ||||
| chr3:160565564-160565830 | Common:2; Rare:89 |