| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75482615-75482617 | |||||
| chr13:76019480-76019763 | Common:2; Rare:69 | ||||
| chr13:76966119-76966373 | Common:4; Rare:52 | ||||
| chr13:77329290-77329327 | Common:2; Rare:11 | ||||
| chr13:77584135-77584471 | Rare:65 | ||||
| chr13:77853758-77854099 | Common:3; Rare:60 | ||||
| chr13:77891511-77891824 | Common:1; Rare:53 | ||||
| chr13:77903210-77903542 | Common:2; Rare:86; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr13:77910619-77910808 | Rare:39 | ||||
| chr13:77914784-77914805 | Common:1; Rare:3 | ||||
| chr13:77920328-77920474 | Common:1; Rare:24 | ||||
| chr13:78029943-78030188 | Rare:32 | ||||
| chr13:78040547-78040710 | Common:1; Rare:27 | ||||
| chr13:79936160-79936195 | Rare:4 | ||||
| chr13:79936766-79937077 | Common:1; Rare:70 |