| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27251282-27251684 | Common:4; Rare:111 | ||||
| chr13:27449953-27450216 | Common:3; Rare:75 | ||||
| chr13:27620567-27620770 | Common:1; Rare:56 | ||||
| chr13:28138835-28139067 | Rare:56 | ||||
| chr13:28139186-28139450 | Rare:61 | ||||
| chr13:28658855-28659228 | Common:2; Rare:137; Clinvar (pathogenic):1 | ||||
| chr13:28659555-28659572 | Rare:4 | ||||
| chr13:29595455-29595562 | Common:1; Rare:30 | ||||
| chr13:30306797-30307204 | Common:7; Rare:111 | ||||
| chr13:30307337-30307575 | Common:2; Rare:78 | ||||
| chr13:30464829-30464971 | Common:1; Rare:53 | ||||
| chr13:30465846-30466109 | Common:1; Rare:82 | ||||
| chr13:30617503-30617993 | Common:1; Rare:161 | ||||
| chr13:31161511-31161577 | Common:1; Rare:24 | ||||
| chr13:32522310-32522596 | Rare:46 |