| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:324493-324622 | Rare:39 | ||||
| chr20:32475292-32475611 | Common:1; Rare:74 | ||||
| chr20:36050894-36051132 | Common:3; Rare:88 | ||||
| chr20:47357802-47358004 | Rare:34 | ||||
| chr21:16194263-16194573 | Common:2; Rare:86 | ||||
| chr21:33945808-33945868 | Common:1; Rare:5 | ||||
| chr21:45994205-45994476 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:22298080-22298196 | Common:2; Rare:41 | ||||
| chr22:23717306-23717516 | Common:1; Rare:66 | ||||
| chr22:30969036-30969292 | Common:2; Rare:73 | ||||
| chr22:46069870-46070072 | Rare:47 | ||||
| chr22:46080057-46080337 | Common:1; Rare:91 | ||||
| chr3:40453175-40453458 | Common:4; Rare:63 | ||||
| chr3:62587250-62587464 | Common:3; Rare:41 | ||||
| chr3:75435012-75435382 | Common:4; Rare:127 |