| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12664058-12664300 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:12796435-12796712 | Common:5; Rare:67 | ||||
| chr3:13480018-13480310 | Common:2; Rare:72 | ||||
| chr3:14124717-14125156 | Common:4; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178532-14178863 | Common:2; Rare:172; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402395-14402700 | Common:1; Rare:78 | ||||
| chr3:14651486-14651801 | Rare:90 | ||||
| chr3:14947239-14947563 | Common:4; Rare:148 | ||||
| chr3:14948052-14948307 | Rare:112 | ||||
| chr3:14948363-14948602 | Common:2; Rare:62 | ||||
| chr3:15099105-15099299 | Rare:50 | ||||
| chr3:15205933-15206282 | Rare:122 | ||||
| chr3:15427510-15427669 | Rare:54 | ||||
| chr3:15601506-15601746 | Common:4; Rare:96 | ||||
| chr3:15859800-15860168 | Common:5; Rare:110 |