| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38872189-38872475 | Rare:77 | ||||
| chr22:39319594-39319752 | Common:3; Rare:75 | ||||
| chr22:40177793-40177940 | Rare:40 | ||||
| chr22:40346434-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40636647-40637033 | Common:2; Rare:107 | ||||
| chr22:40819283-40819491 | Common:11; Rare:106 | ||||
| chr22:40856917-40857159 | Common:1; Rare:100; Clinvar:3 | ||||
| chr22:40951574-40951716 | Common:2; Rare:46 | ||||
| chr22:41286142-41286541 | Common:2; Rare:129 | ||||
| chr22:41446785-41446963 | Rare:73 | ||||
| chr22:41468697-41469159 | Rare:116 | ||||
| chr22:41621000-41621377 | Common:7; Rare:138 | ||||
| chr22:41621739-41621807 | Rare:20 | ||||
| chr22:41800545-41800688 | Common:1; Rare:40 | ||||
| chr22:41832828-41833327 | Common:3; Rare:165 |