| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42649327-42649532 | Common:3; Rare:82 | ||||
| chr22:42857184-42857443 | Common:3; Rare:106 | ||||
| chr22:43015098-43015384 | Common:2; Rare:117 | ||||
| chr22:43812223-43812441 | Common:3; Rare:73 | ||||
| chr22:43923555-43923818 | Common:4; Rare:74; Clinvar (benign):3 | ||||
| chr22:43955303-43955562 | Common:3; Rare:79 | ||||
| chr22:44498172-44498475 | Common:2; Rare:115 | ||||
| chr22:45163747-45164023 | Common:3; Rare:107 | ||||
| chr22:45309656-45309964 | Common:1; Rare:129 | ||||
| chr22:45502762-45502988 | Common:1; Rare:72 | ||||
| chr22:46250278-46250408 | Common:1; Rare:42 | ||||
| chr22:46267826-46268042 | Common:1; Rare:66 | ||||
| chr22:46296560-46296922 | Common:2; Rare:110 | ||||
| chr22:46335584-46335804 | Common:6; Rare:99; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr22:46762455-46762701 | Common:3; Rare:92 |