| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:25301502-25301696 | Common:1; Rare:77 | ||||
| chr13:26221787-26221953 | Rare:47 | ||||
| chr13:26222183-26222365 | Common:3; Rare:52 | ||||
| chr13:27251235-27251626 | Common:8; Rare:121 | ||||
| chr13:27450037-27450207 | Common:2; Rare:51 | ||||
| chr13:27450377-27450627 | Common:4; Rare:101 | ||||
| chr13:27620465-27620812 | Common:2; Rare:117 | ||||
| chr13:28138119-28138234 | Common:1; Rare:38 | ||||
| chr13:28659076-28659181 | Rare:47; Clinvar (pathogenic):1 | ||||
| chr13:30617277-30618000 | Common:1; Rare:224 | ||||
| chr13:31162341-31162454 | Common:1; Rare:27 | ||||
| chr13:32031255-32031328 | Common:1; Rare:21 | ||||
| chr13:32031554-32031777 | Common:1; Rare:61 | ||||
| chr13:32315415-32315531 | Rare:31; Clinvar:1 | ||||
| chr13:32586234-32586582 | Common:2; Rare:104 |