| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110302426-110302721 | Common:7; Rare:34 | ||||
| chr13:110305195-110305243 | Rare:10 | ||||
| chr13:110308494-110308596 | Common:1; Rare:22 | ||||
| chr13:110312070-110312339 | Common:4; Rare:57 | ||||
| chr13:110316798-110316871 | Rare:18 | ||||
| chr13:110318776-110319048 | Common:1; Rare:45 | ||||
| chr13:110372132-110372247 | Rare:22 | ||||
| chr13:110400524-110400631 | Common:2; Rare:16 | ||||
| chr13:110403368-110403598 | Common:4; Rare:28 | ||||
| chr13:110407634-110407805 | Common:3; Rare:29 | ||||
| chr13:110408041-110408365 | Common:4; Rare:59 | ||||
| chr13:110408625-110408777 | Common:3; Rare:41 | ||||
| chr13:110409520-110409627 | Common:1; Rare:17 | ||||
| chr13:110409880-110410015 | Common:2; Rare:29 | ||||
| chr13:110424729-110424993 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):2 |