| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41560834-41560873 | Rare:8 | ||||
| chr22:41560883-41561162 | Common:9; Rare:78 | ||||
| chr22:41620751-41620822 | Rare:31 | ||||
| chr22:41620973-41621384 | Common:7; Rare:144 | ||||
| chr22:41800517-41800720 | Common:1; Rare:63 | ||||
| chr22:41832649-41832701 | Rare:9 | ||||
| chr22:41832909-41833355 | Common:3; Rare:149 | ||||
| chr22:42070744-42070971 | Common:2; Rare:51 | ||||
| chr22:42079499-42079808 | Common:2; Rare:88 | ||||
| chr22:42090617-42091069 | Common:2; Rare:178; Clinvar (pathogenic):1 | ||||
| chr22:42210634-42210926 | Rare:85 | ||||
| chr22:42614850-42615251 | Common:3; Rare:168 | ||||
| chr22:42649302-42649495 | Common:1; Rare:76 | ||||
| chr22:42720813-42720975 | Rare:49 | ||||
| chr22:42857156-42857317 | Common:2; Rare:65 |