| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41621018-41621360 | Common:7; Rare:129 | ||||
| chr22:41832909-41833139 | Common:3; Rare:75 | ||||
| chr22:42070770-42070948 | Common:2; Rare:38 | ||||
| chr22:42090735-42090967 | Common:1; Rare:80; Clinvar (pathogenic):1 | ||||
| chr22:42614858-42615246 | Common:3; Rare:161 | ||||
| chr22:42649320-42649479 | Common:1; Rare:63 | ||||
| chr22:43955275-43955562 | Common:3; Rare:87 | ||||
| chr22:45309676-45309975 | Common:1; Rare:122 | ||||
| chr22:45413571-45413742 | Rare:72 | ||||
| chr22:46053786-46053909 | Rare:42 | ||||
| chr22:46250268-46250408 | Common:1; Rare:45 | ||||
| chr22:46267883-46268032 | Common:1; Rare:47 | ||||
| chr22:46762506-46762676 | Common:3; Rare:61 | ||||
| chr22:50185690-50185949 | Common:4; Rare:109 | ||||
| chr22:50244949-50245114 | Common:2; Rare:63 |