| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41560883-41561152 | Common:9; Rare:76 | ||||
| chr22:41620992-41621380 | Common:7; Rare:140 | ||||
| chr22:41656743-41657029 | Common:1; Rare:65 | ||||
| chr22:41800532-41800631 | Rare:30 | ||||
| chr22:41832838-41833355 | Common:3; Rare:171 | ||||
| chr22:41947093-41947203 | Rare:41 | ||||
| chr22:42070770-42070935 | Common:1; Rare:35 | ||||
| chr22:42079505-42079783 | Common:2; Rare:75 | ||||
| chr22:42090597-42091054 | Common:2; Rare:183; Clinvar (pathogenic):1 | ||||
| chr22:42519771-42519874 | Common:1; Rare:45 | ||||
| chr22:42553728-42553934 | Common:1; Rare:60 | ||||
| chr22:42614858-42615246 | Common:3; Rare:161 | ||||
| chr22:42644594-42644837 | Common:8; Rare:58 | ||||
| chr22:42646661-42646927 | Common:1; Rare:58 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 |