| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39153543-39153767 | Common:6; Rare:151 | ||||
| chr3:39154556-39154693 | Rare:63 | ||||
| chr3:39383286-39383464 | Common:4; Rare:68; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:39383539-39383680 | Rare:56; Clinvar:3 | ||||
| chr3:39406573-39406767 | Common:4; Rare:157 | ||||
| chr3:40309448-40309915 | Common:18; Rare:290 | ||||
| chr3:40457202-40457400 | Common:6; Rare:185 | ||||
| chr3:40477083-40477224 | Common:1; Rare:39 | ||||
| chr3:40505853-40506151 | Rare:145 | ||||
| chr3:40524812-40525028 | Common:1; Rare:112 | ||||
| chr3:41199358-41199665 | Common:3; Rare:209 | ||||
| chr3:41199860-41200160 | Common:3; Rare:148 | ||||
| chr3:41277640-41277870 | Rare:49 | ||||
| chr3:41278105-41278407 | Common:1; Rare:84 | ||||
| chr3:42013452-42013837 | Common:11; Rare:185 |