| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31981634-31981780 | Rare:39 | ||||
| chr3:32106380-32106697 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570672-32570914 | Rare:112 | ||||
| chr3:32685051-32685386 | Rare:102 | ||||
| chr3:33277294-33277489 | Common:2; Rare:51 | ||||
| chr3:33798514-33798701 | Common:2; Rare:67 | ||||
| chr3:33798985-33799213 | Rare:72 | ||||
| chr3:36993073-36993569 | Common:2; Rare:170; Clinvar:28; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr3:37176131-37176389 | Rare:72 | ||||
| chr3:37243172-37243392 | Common:1; Rare:54 | ||||
| chr3:38024475-38024667 | Common:1; Rare:73 | ||||
| chr3:38029612-38029864 | Common:1; Rare:51 | ||||
| chr3:39051944-39052052 | Common:1; Rare:40 | ||||
| chr3:39107568-39107725 | Common:3; Rare:48 | ||||
| chr3:39383270-39383441 | Common:2; Rare:30; Clinvar:2; Clinvar (benign):1 |