| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:28442910-28443659 | Common:4; Rare:221 | ||||
| chr22:28679660-28680130 | Common:17; Rare:422 | ||||
| chr22:28741584-28742127 | Common:16; Rare:656; Clinvar:16; Clinvar (benign):41 | ||||
| chr22:28742381-28742840 | Common:6; Rare:450 | ||||
| chr22:28772420-28772840 | Common:24; Rare:301 | ||||
| chr22:28772893-28773293 | Common:5; Rare:126 | ||||
| chr22:28773276-28773511 | Common:4; Rare:59 | ||||
| chr22:28799439-28800337 | Common:10; Rare:563 | ||||
| chr22:28800360-28800880 | Common:36; Rare:834 | ||||
| chr22:28883065-28883986 | Common:35; Rare:949 | ||||
| chr22:29072719-29073119 | Common:4; Rare:207 | ||||
| chr22:29205565-29206111 | Common:5; Rare:569 | ||||
| chr22:29267703-29268437 | Common:20; Rare:1103 | ||||
| chr22:29268460-29269150 | Common:4; Rare:466 | ||||
| chr22:29306113-29306513 | Common:2; Rare:246 |