| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46576740-46577194 | Common:12; Rare:275 | ||||
| chr22:46738205-46738417 | Common:5; Rare:54 | ||||
| chr22:46762453-46762707 | Common:6; Rare:189 | ||||
| chr22:49827801-49827964 | Common:2; Rare:111 | ||||
| chr22:49853485-49853913 | Common:4; Rare:304 | ||||
| chr22:49917830-49918320 | Common:11; Rare:193 | ||||
| chr22:49918271-49918778 | Common:9; Rare:303; Clinvar (benign):3 | ||||
| chr22:49960231-49960829 | Common:12; Rare:409 | ||||
| chr22:50169930-50170340 | Common:3; Rare:111 | ||||
| chr22:50185690-50185953 | Common:8; Rare:210 | ||||
| chr22:50200797-50201046 | Common:10; Rare:191 | ||||
| chr22:50244320-50244740 | Common:4; Rare:209; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:50244939-50245133 | Common:3; Rare:125 | ||||
| chr22:50261446-50261936 | Common:4; Rare:188 | ||||
| chr22:50270334-50270574 | Common:1; Rare:68 |