| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53842090-53842420 | Common:2; Rare:59 | ||||
| chr19:53889765-53889904 | Rare:35; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:53889974-53890212 | Common:2; Rare:76; Clinvar:2 | ||||
| chr19:53979955-53980488 | Common:15; Rare:147 | ||||
| chr19:53981263-53981451 | Rare:48 | ||||
| chr19:54020139-54020314 | Common:1; Rare:30 | ||||
| chr19:54095901-54096312 | Common:10; Rare:230 | ||||
| chr19:54136967-54137178 | Common:4; Rare:48 | ||||
| chr19:54231773-54231951 | Rare:31 | ||||
| chr19:54359368-54359622 | Common:1; Rare:28 | ||||
| chr19:54431602-54431785 | Common:2; Rare:32 | ||||
| chr19:54448116-54448235 | Common:1; Rare:25 | ||||
| chr19:54464406-54464566 | Common:3; Rare:56 | ||||
| chr19:54464691-54464954 | Common:3; Rare:107 | ||||
| chr19:55006063-55006312 | Common:3; Rare:96 |