| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30464250-30464268 | Rare:8 | ||||
| chr13:30465795-30466134 | Common:1; Rare:107 | ||||
| chr13:30617565-30617855 | Common:1; Rare:96 | ||||
| chr13:30735395-30735665 | Common:2; Rare:66 | ||||
| chr13:32315426-32315531 | Rare:29; Clinvar:1 | ||||
| chr13:32538728-32539003 | Common:1; Rare:69 | ||||
| chr13:32586253-32586574 | Common:2; Rare:97 | ||||
| chr13:33818024-33818258 | Common:1; Rare:110 | ||||
| chr13:35476687-35476841 | Common:1; Rare:22 | ||||
| chr13:36999296-36999602 | Common:1; Rare:90 | ||||
| chr13:37000712-37000815 | Rare:43; Clinvar (pathogenic):1 | ||||
| chr13:37059585-37059737 | Common:1; Rare:51 | ||||
| chr13:39038087-39038439 | Common:1; Rare:87 | ||||
| chr13:39655605-39655754 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:40771132-40771328 | Common:3; Rare:60 |