| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33798435-33798686 | Common:2; Rare:81 | ||||
| chr3:33799006-33799049 | Rare:17 | ||||
| chr3:36993062-36993563 | Common:2; Rare:169; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176182-37176393 | Rare:61 | ||||
| chr3:37243024-37243369 | Common:5; Rare:91 | ||||
| chr3:38024475-38024667 | Common:1; Rare:73 | ||||
| chr3:38138549-38138703 | Common:2; Rare:60; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:38165759-38165822 | Rare:20 | ||||
| chr3:39051944-39052057 | Common:1; Rare:42 | ||||
| chr3:39107531-39107704 | Common:3; Rare:54 | ||||
| chr3:39153495-39153750 | Common:3; Rare:81 | ||||
| chr3:39383325-39383657 | Common:3; Rare:77; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:39809337-39809697 | Common:3; Rare:116 | ||||
| chr3:40309457-40309819 | Common:9; Rare:122 | ||||
| chr3:40457223-40457376 | Common:3; Rare:74 |