| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40636612-40637069 | Common:7; Rare:343 | ||||
| chr22:40819231-40819601 | Common:33; Rare:385 | ||||
| chr22:40856433-40857227 | Common:7; Rare:800; Clinvar:11 | ||||
| chr22:40950976-40951432 | Common:6; Rare:406 | ||||
| chr22:40951538-40951913 | Common:9; Rare:264 | ||||
| chr22:41091288-41092040 | Common:24; Rare:638 | ||||
| chr22:41092272-41092913 | Rare:242; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:41285820-41286090 | Common:2; Rare:112 | ||||
| chr22:41286103-41286623 | Common:6; Rare:461 | ||||
| chr22:41301459-41301847 | Rare:140 | ||||
| chr22:41367063-41367520 | Rare:328 | ||||
| chr22:41381188-41381600 | Common:18; Rare:382 | ||||
| chr22:41381649-41382008 | Common:10; Rare:289 | ||||
| chr22:41446160-41446700 | Common:4; Rare:162 | ||||
| chr22:41446767-41447070 | Common:1; Rare:218 |