| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50525543-50525663 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50532484-50532667 | Common:2; Rare:43 | ||||
| chr22:50562857-50563053 | Common:3; Rare:55 | ||||
| chr22:50577884-50578332 | Common:2; Rare:144 | ||||
| chr22:50580034-50580245 | Common:2; Rare:67; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr22:50582400-50582570 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:50582779-50583142 | Common:7; Rare:123; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50601177-50601267 | Common:2; Rare:22 | ||||
| chr22:50627989-50628313 | Common:9; Rare:134; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:50738081-50738274 | Common:3; Rare:47 | ||||
| chr22:50783565-50783859 | Common:2; Rare:99 | ||||
| chr3:197230-197296 | Rare:24 | ||||
| chr3:2892163-2892269 | Common:3; Rare:21 | ||||
| chr3:3126768-3127075 | Common:4; Rare:129; Clinvar (benign):4 | ||||
| chr3:3179629-3179792 | Common:1; Rare:80; Clinvar:4 |