| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40009464-40009762 | Common:5; Rare:88 | ||||
| chr22:40009951-40010102 | Rare:34 | ||||
| chr22:40044138-40044421 | Common:4; Rare:130 | ||||
| chr22:40044552-40044883 | Common:4; Rare:138 | ||||
| chr22:40045219-40045790 | Common:6; Rare:231 | ||||
| chr22:40177793-40177951 | Rare:85 | ||||
| chr22:40346395-40346572 | Common:1; Rare:145; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr22:40636633-40637033 | Common:4; Rare:220 | ||||
| chr22:40819266-40819529 | Common:22; Rare:230 | ||||
| chr22:40856394-40856724 | Common:1; Rare:277 | ||||
| chr22:40856726-40857182 | Common:5; Rare:262; Clinvar:8 | ||||
| chr22:40951085-40951397 | Common:2; Rare:105 | ||||
| chr22:40951400-40951580 | Rare:49 | ||||
| chr22:40951500-40951970 | Common:5; Rare:197 | ||||
| chr22:41091398-41092048 | Common:14; Rare:362 |