| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45692395-45692695 | Common:1; Rare:68 | ||||
| chr19:45730853-45731027 | Common:1; Rare:37 | ||||
| chr19:45768247-45768494 | Rare:106; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45769145-45769319 | Rare:51 | ||||
| chr19:45772734-45772859 | Common:1; Rare:29 | ||||
| chr19:45863088-45863376 | Common:4; Rare:97 | ||||
| chr19:45864139-45864375 | Common:2; Rare:54 | ||||
| chr19:46023050-46023186 | Common:1; Rare:32 | ||||
| chr19:46296790-46297069 | Common:4; Rare:108 | ||||
| chr19:46298120-46298463 | Common:5; Rare:84 | ||||
| chr19:46303420-46303675 | Common:1; Rare:43 | ||||
| chr19:46346929-46347192 | Common:3; Rare:89 | ||||
| chr19:46471484-46471650 | Common:5; Rare:64 | ||||
| chr19:46495846-46496039 | Rare:55 | ||||
| chr19:46600913-46601434 | Common:6; Rare:179; Clinvar (benign):3 |