| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30617303-30618180 | Common:3; Rare:645 | ||||
| chr13:30618380-30618525 | Common:2; Rare:40 | ||||
| chr13:31161348-31161748 | Common:5; Rare:220 | ||||
| chr13:31161804-31162214 | Common:3; Rare:459 | ||||
| chr13:31162260-31162589 | Common:6; Rare:219 | ||||
| chr13:31199813-31200133 | Common:3; Rare:314 | ||||
| chr13:31200168-31200730 | Common:7; Rare:348 | ||||
| chr13:32031129-32031264 | Common:1; Rare:34 | ||||
| chr13:32031261-32031425 | Common:1; Rare:45 | ||||
| chr13:32031462-32031797 | Common:2; Rare:137 | ||||
| chr13:32315171-32315618 | Common:5; Rare:220; Clinvar:6; Clinvar (benign):7 | ||||
| chr13:32315693-32316066 | Common:6; Rare:126; Clinvar (benign):7 | ||||
| chr13:32428086-32428292 | Rare:81 | ||||
| chr13:32538593-32538993 | Common:3; Rare:215 | ||||
| chr13:32586179-32586648 | Common:4; Rare:272 |