| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41832909-41833231 | Common:3; Rare:110 | ||||
| chr22:42070531-42070987 | Common:4; Rare:105; Clinvar:1 | ||||
| chr22:42079463-42079757 | Common:2; Rare:75 | ||||
| chr22:42090733-42090947 | Common:1; Rare:77; Clinvar (pathogenic):1 | ||||
| chr22:42432340-42432511 | Rare:40 | ||||
| chr22:42614800-42615259 | Common:5; Rare:204 | ||||
| chr22:42857215-42857477 | Common:2; Rare:109 | ||||
| chr22:43015054-43015385 | Common:2; Rare:130 | ||||
| chr22:43151418-43151618 | Common:2; Rare:45 | ||||
| chr22:44023943-44024006 | Common:1; Rare:12 | ||||
| chr22:44068808-44069144 | Common:2; Rare:75 | ||||
| chr22:44181153-44181184 | Rare:8 | ||||
| chr22:44181236-44181434 | Common:3; Rare:50 | ||||
| chr22:45163674-45163942 | Common:4; Rare:94 | ||||
| chr22:45309676-45309990 | Common:1; Rare:124 |