| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27620443-27620812 | Common:2; Rare:125 | ||||
| chr13:28658872-28659184 | Common:1; Rare:118; Clinvar (pathogenic):1 | ||||
| chr13:28718787-28719123 | Common:1; Rare:86 | ||||
| chr13:30306821-30307207 | Common:7; Rare:106 | ||||
| chr13:30464246-30464342 | Rare:31 | ||||
| chr13:30617479-30618000 | Common:1; Rare:171 | ||||
| chr13:32254005-32254320 | Common:2; Rare:69 | ||||
| chr13:33285625-33285884 | Common:1; Rare:65 | ||||
| chr13:35476659-35476841 | Common:1; Rare:26 | ||||
| chr13:36346258-36346453 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000544-37000815 | Common:2; Rare:89; Clinvar (pathogenic):1 | ||||
| chr13:37059602-37059726 | Common:1; Rare:43 | ||||
| chr13:38350249-38350365 | Rare:34 | ||||
| chr13:39038087-39038426 | Common:1; Rare:87 | ||||
| chr13:39603127-39603316 | Common:1; Rare:67 |