| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197958780-197959458 | Common:6; Rare:162 | ||||
| chr3:197959628-197960364 | Common:9; Rare:953 | ||||
| chr3:197960430-197960562 | Rare:26 | ||||
| chr3:197960466-197961108 | Common:8; Rare:235 | ||||
| chr4:53030-53350 | Rare:5 | ||||
| chr4:124199-124599 | Common:20; Rare:229 | ||||
| chr4:124704-125179 | Common:6; Rare:224 | ||||
| chr4:304776-305763 | Common:6; Rare:455 | ||||
| chr4:474079-474483 | Common:12; Rare:430 | ||||
| chr4:499049-499487 | Common:20; Rare:694; Clinvar (benign):1 | ||||
| chr4:673242-674092 | Common:10; Rare:1150 | ||||
| chr4:674211-674616 | Common:18; Rare:1144 | ||||
| chr4:680901-681887 | Common:14; Rare:1099 | ||||
| chr4:687052-687615 | Common:7; Rare:733 | ||||
| chr4:687651-688089 | Common:4; Rare:193 |