| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134545440-134545674 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:135965534-135965847 | Common:1; Rare:124 | ||||
| chr3:136195811-136195997 | Common:1; Rare:77 | ||||
| chr3:136196492-136196938 | Rare:153 | ||||
| chr3:136250258-136250378 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:136250514-136250711 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:136752322-136752707 | Common:1; Rare:122 | ||||
| chr3:136862000-136862306 | Common:1; Rare:98 | ||||
| chr3:138174833-138174997 | Common:2; Rare:37 | ||||
| chr3:138187226-138187602 | Rare:116 | ||||
| chr3:138348378-138348692 | Common:2; Rare:81 | ||||
| chr3:138434455-138434653 | Common:4; Rare:71 | ||||
| chr3:138594193-138594451 | Rare:75 | ||||
| chr3:138608489-138608808 | Rare:68 | ||||
| chr3:138608972-138609081 | Rare:33 |