| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39349820-39350017 | Common:1; Rare:59 | ||||
| chr22:39502158-39502412 | Rare:75 | ||||
| chr22:39521045-39521834 | Common:7; Rare:321 | ||||
| chr22:39532667-39532888 | Common:2; Rare:97 | ||||
| chr22:40043980-40044346 | Common:2; Rare:80 | ||||
| chr22:40044887-40044995 | Common:1; Rare:31 | ||||
| chr22:40346433-40346585 | Rare:71; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636621-40637012 | Common:2; Rare:114 | ||||
| chr22:40819311-40819515 | Common:11; Rare:102 | ||||
| chr22:40856424-40857167 | Common:3; Rare:302; Clinvar:4 | ||||
| chr22:40951015-40951417 | Common:2; Rare:138 | ||||
| chr22:40951559-40951716 | Common:2; Rare:49 | ||||
| chr22:41091413-41091847 | Common:6; Rare:160 | ||||
| chr22:41286141-41286424 | Common:2; Rare:92 | ||||
| chr22:41446446-41446541 | Rare:18 |