| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762417-46762705 | Common:4; Rare:115 | ||||
| chr22:46763055-46763329 | Common:4; Rare:74 | ||||
| chr22:46773845-46773917 | Rare:14 | ||||
| chr22:46774204-46774595 | Rare:74 | ||||
| chr22:49827750-49828006 | Common:1; Rare:97 | ||||
| chr22:49853377-49853992 | Common:2; Rare:200 | ||||
| chr22:49918145-49918239 | Rare:25 | ||||
| chr22:49918254-49918264 | Rare:1 | ||||
| chr22:49918270-49918797 | Common:7; Rare:182; Clinvar (benign):3 | ||||
| chr22:49960099-49960608 | Common:5; Rare:197 | ||||
| chr22:49960668-49960883 | Common:2; Rare:99 | ||||
| chr22:50185638-50186018 | Common:7; Rare:135 | ||||
| chr22:50190363-50191173 | Common:11; Rare:213 | ||||
| chr22:50192528-50192676 | Common:1; Rare:31 | ||||
| chr22:50192946-50193128 | Rare:48 |