| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46249564-46249964 | Rare:140 | ||||
| chr22:46250127-46250590 | Common:23; Rare:648 | ||||
| chr22:46250960-46251360 | Common:1; Rare:93 | ||||
| chr22:46267659-46268059 | Common:8; Rare:439 | ||||
| chr22:46268494-46268894 | Common:5; Rare:129 | ||||
| chr22:46296200-46297010 | Common:15; Rare:699 | ||||
| chr22:46335495-46335961 | Common:38; Rare:746; Clinvar:57; Clinvar (benign):62; Clinvar (pathogenic):8 | ||||
| chr22:46336096-46336550 | Common:12; Rare:373 | ||||
| chr22:46576421-46577228 | Common:12; Rare:523 | ||||
| chr22:46619699-46620099 | Common:6; Rare:158 | ||||
| chr22:46737618-46738506 | Common:33; Rare:430 | ||||
| chr22:46762387-46762957 | Common:25; Rare:849 | ||||
| chr22:46763039-46763619 | Common:8; Rare:202 | ||||
| chr22:49826837-49827653 | Common:10; Rare:347 | ||||
| chr22:49827790-49828080 | Common:6; Rare:265 |