| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:19958468-19958840 | Common:6; Rare:172 | ||||
| chr13:21140442-21140634 | Rare:97 | ||||
| chr13:21146895-21147252 | Common:2; Rare:71 | ||||
| chr13:21176478-21176697 | Common:2; Rare:94 | ||||
| chr13:23889339-23889586 | Common:1; Rare:85 | ||||
| chr13:24512726-24512862 | Common:3; Rare:40 | ||||
| chr13:26221710-26221864 | Rare:44 | ||||
| chr13:27251268-27251618 | Common:4; Rare:100 | ||||
| chr13:27620548-27620810 | Common:1; Rare:79 | ||||
| chr13:28137907-28138417 | Common:4; Rare:127 | ||||
| chr13:28658864-28659183 | Common:1; Rare:120; Clinvar (pathogenic):1 | ||||
| chr13:29850280-29850358 | Common:1; Rare:23 | ||||
| chr13:29850527-29850596 | Common:1; Rare:24 | ||||
| chr13:30306968-30307197 | Common:5; Rare:54 | ||||
| chr13:30617605-30617988 | Common:1; Rare:120 |