| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28659036-28659185 | Rare:71; Clinvar (pathogenic):1 | ||||
| chr13:28819667-28820067 | Common:31; Rare:280 | ||||
| chr13:29595634-29595899 | Common:2; Rare:95 | ||||
| chr13:29850465-29850582 | Common:2; Rare:25 | ||||
| chr13:30306970-30307266 | Common:5; Rare:84 | ||||
| chr13:30307414-30307643 | Common:3; Rare:71 | ||||
| chr13:30464470-30465090 | Common:6; Rare:207 | ||||
| chr13:30465911-30466371 | Common:2; Rare:114 | ||||
| chr13:30616927-30617166 | Rare:49 | ||||
| chr13:30617418-30617982 | Common:1; Rare:186 | ||||
| chr13:30618262-30618496 | Common:2; Rare:38 | ||||
| chr13:31162366-31162589 | Common:2; Rare:65 | ||||
| chr13:31199854-31199986 | Common:1; Rare:42 | ||||
| chr13:31200233-31200384 | Common:2; Rare:49 | ||||
| chr13:32030933-32031333 | Common:5; Rare:120 |