| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762496-46762713 | Common:3; Rare:82 | ||||
| chr22:50190434-50190614 | Common:2; Rare:56 | ||||
| chr22:50244632-50244637 | Rare:1 | ||||
| chr22:50244954-50245058 | Common:2; Rare:40 | ||||
| chr22:50280551-50280920 | Common:3; Rare:117 | ||||
| chr22:50282185-50282429 | Common:3; Rare:77 | ||||
| chr22:50525524-50525681 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50532140-50532196 | Rare:12 | ||||
| chr22:50562868-50563044 | Common:3; Rare:52 | ||||
| chr22:50582380-50582452 | Rare:37 | ||||
| chr22:50582779-50583121 | Common:7; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50601224-50601272 | Common:1; Rare:12 | ||||
| chr22:50628046-50628274 | Common:9; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783587-50783859 | Common:2; Rare:90 | ||||
| chr3:196994-197334 | Common:3; Rare:122 |