| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45793316-45793754 | Common:5; Rare:93 | ||||
| chr22:46250268-46250413 | Common:2; Rare:46 | ||||
| chr22:46296738-46296918 | Common:1; Rare:61 | ||||
| chr22:46335601-46335797 | Common:5; Rare:91; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762436-46762701 | Common:4; Rare:103 | ||||
| chr22:48489277-48489586 | Common:2; Rare:119 | ||||
| chr22:50244942-50245119 | Common:2; Rare:66 | ||||
| chr22:50270321-50270496 | Common:1; Rare:53 | ||||
| chr22:50286051-50286237 | Common:1; Rare:60 | ||||
| chr22:50326933-50327202 | Common:3; Rare:89 | ||||
| chr22:50562887-50563053 | Common:3; Rare:46 | ||||
| chr22:50582365-50582606 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:50582777-50583151 | Common:8; Rare:131; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50600426-50600866 | Rare:112 | ||||
| chr22:50628082-50628313 | Common:9; Rare:110; Clinvar:3; Clinvar (benign):1 |