| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:44024189-44024369 | Common:1; Rare:60 | ||||
| chr22:44026289-44026348 | Rare:16 | ||||
| chr22:44498179-44498479 | Common:2; Rare:116 | ||||
| chr22:45163781-45164014 | Common:2; Rare:83 | ||||
| chr22:45309669-45309972 | Common:1; Rare:125 | ||||
| chr22:46053778-46053895 | Rare:41 | ||||
| chr22:46250268-46250408 | Common:1; Rare:45 | ||||
| chr22:46296666-46296918 | Common:2; Rare:92 | ||||
| chr22:46335601-46335799 | Common:5; Rare:91; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762512-46762669 | Common:3; Rare:54 | ||||
| chr22:50185678-50185953 | Common:5; Rare:111 | ||||
| chr22:50244949-50245091 | Common:2; Rare:54 | ||||
| chr22:50525530-50525723 | Common:4; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50582784-50583121 | Common:7; Rare:105; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628073-50628270 | Common:8; Rare:93; Clinvar:3; Clinvar (benign):1 |