| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20982220-20982336 | Common:1; Rare:24; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:23894317-23894826 | Common:6; Rare:196 | ||||
| chr22:24554998-24555474 | Common:4; Rare:179 | ||||
| chr22:24555794-24556014 | Rare:68 | ||||
| chr22:26512439-26512552 | Common:1; Rare:51 | ||||
| chr22:27919195-27919504 | Common:5; Rare:139 | ||||
| chr22:28741800-28742091 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28800349-28800689 | Common:5; Rare:124 | ||||
| chr22:29267835-29268334 | Common:2; Rare:145 | ||||
| chr22:29766948-29767401 | Common:5; Rare:127 | ||||
| chr22:30356871-30357040 | Common:2; Rare:51 | ||||
| chr22:30607039-30607258 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:31160159-31160243 | Rare:32 | ||||
| chr22:32412167-32412353 | Common:2; Rare:58 | ||||
| chr22:37019415-37019848 | Common:5; Rare:127 |