| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37849301-37849480 | Rare:106 | ||||
| chr22:37953550-37953725 | Rare:67 | ||||
| chr22:38181793-38182024 | Common:2; Rare:59 | ||||
| chr22:38506275-38506651 | Common:1; Rare:122 | ||||
| chr22:38570184-38570483 | Common:5; Rare:53 | ||||
| chr22:38656372-38656682 | Common:1; Rare:79 | ||||
| chr22:38681821-38682030 | Common:2; Rare:88 | ||||
| chr22:39319604-39319779 | Common:2; Rare:76 | ||||
| chr22:40346476-40346551 | Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:40856812-40857154 | Common:2; Rare:132; Clinvar:3 | ||||
| chr22:41286167-41286424 | Common:2; Rare:79 | ||||
| chr22:41621012-41621361 | Common:7; Rare:131 | ||||
| chr22:41832909-41833131 | Common:3; Rare:71 | ||||
| chr22:41940220-41940382 | Common:1; Rare:29 | ||||
| chr22:42070802-42070948 | Common:2; Rare:31 |