| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45671822-45672076 | Common:2; Rare:97 | ||||
| chr22:46053767-46053909 | Rare:53 | ||||
| chr22:46150289-46150651 | Common:1; Rare:117 | ||||
| chr22:46150968-46151110 | Rare:20 | ||||
| chr22:46171077-46171398 | Common:4; Rare:48 | ||||
| chr22:46171419-46171558 | Common:1; Rare:26 | ||||
| chr22:46250254-46250423 | Common:3; Rare:55 | ||||
| chr22:46267832-46268071 | Common:1; Rare:80 | ||||
| chr22:46296750-46296918 | Rare:54 | ||||
| chr22:46335621-46335813 | Common:5; Rare:90; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46738046-46738368 | Common:6; Rare:82 | ||||
| chr22:46762453-46762718 | Common:3; Rare:100 | ||||
| chr22:49853576-49853921 | Common:2; Rare:127 | ||||
| chr22:50185690-50185953 | Common:4; Rare:110 | ||||
| chr22:50225923-50226053 | Common:1; Rare:46; Clinvar (pathogenic):1 |