| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:19958476-19958846 | Common:6; Rare:172 | ||||
| chr13:20160939-20161142 | Rare:69; Clinvar (benign):1 | ||||
| chr13:20525796-20525941 | Common:1; Rare:60 | ||||
| chr13:20566794-20567197 | Common:1; Rare:113 | ||||
| chr13:20773912-20774181 | Common:4; Rare:90 | ||||
| chr13:21140398-21140681 | Rare:121 | ||||
| chr13:21176484-21176716 | Common:2; Rare:105 | ||||
| chr13:21604106-21604226 | Common:4; Rare:74 | ||||
| chr13:21670946-21671085 | Common:1; Rare:42 | ||||
| chr13:23180811-23181034 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr13:23570294-23570570 | Common:1; Rare:56 | ||||
| chr13:23579236-23579407 | Common:3; Rare:54 | ||||
| chr13:23889302-23889476 | Rare:65 | ||||
| chr13:24160528-24160798 | Common:1; Rare:81 | ||||
| chr13:24270671-24270794 | Common:1; Rare:24 |