| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50074791-50074947 | Common:1; Rare:38 | ||||
| chr22:50085238-50085495 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50185704-50185949 | Common:4; Rare:103 | ||||
| chr22:50244964-50245059 | Common:2; Rare:36 | ||||
| chr22:50525538-50525685 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50582806-50583120 | Common:6; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:50628098-50628267 | Common:8; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783616-50783854 | Common:2; Rare:71 | ||||
| chr3:197162-197318 | Rare:51 | ||||
| chr3:4303247-4303412 | Common:2; Rare:66 | ||||
| chr3:4493177-4493382 | Rare:76; Clinvar:1 | ||||
| chr3:4979290-4979714 | Common:3; Rare:97 | ||||
| chr3:4979747-4980136 | Common:1; Rare:122 | ||||
| chr3:4980388-4980489 | Rare:30 | ||||
| chr3:8501641-8501947 | Common:2; Rare:112 |