| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37242884-37243189 | Common:5; Rare:85 | ||||
| chr3:37243208-37243429 | Common:1; Rare:51 | ||||
| chr3:37861719-37861842 | Rare:34 | ||||
| chr3:38024453-38024671 | Common:1; Rare:83 | ||||
| chr3:38029605-38029788 | Common:1; Rare:36 | ||||
| chr3:38138549-38138733 | Common:2; Rare:71; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051944-39052073 | Common:1; Rare:49 | ||||
| chr3:39107545-39107684 | Common:2; Rare:45 | ||||
| chr3:39153539-39153714 | Common:3; Rare:58 | ||||
| chr3:39383281-39383452 | Common:2; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383561-39383694 | Rare:33; Clinvar:2 | ||||
| chr3:39406577-39406758 | Common:2; Rare:78 | ||||
| chr3:40309452-40309914 | Common:9; Rare:154 | ||||
| chr3:40457204-40457470 | Common:6; Rare:123 | ||||
| chr3:40477083-40477184 | Common:1; Rare:28 |