| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46296699-46296924 | Common:2; Rare:79 | ||||
| chr22:46335621-46335819 | Common:5; Rare:92; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762455-46762718 | Common:3; Rare:99 | ||||
| chr22:46916028-46916198 | Common:3; Rare:25 | ||||
| chr22:49853592-49853904 | Common:2; Rare:114 | ||||
| chr22:49918408-49918741 | Common:2; Rare:124 | ||||
| chr22:50089750-50090282 | Common:12; Rare:191 | ||||
| chr22:50185725-50185942 | Common:4; Rare:91 | ||||
| chr22:50244632-50244676 | Rare:11 | ||||
| chr22:50244954-50245070 | Common:2; Rare:45 | ||||
| chr22:50282239-50282514 | Common:5; Rare:79 | ||||
| chr22:50307566-50307881 | Common:9; Rare:61 | ||||
| chr22:50505786-50506073 | Common:4; Rare:137 | ||||
| chr22:50507641-50508042 | Common:2; Rare:102 | ||||
| chr22:50508189-50508267 | Rare:24 |