| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50362968-50363422 | Common:3; Rare:184 | ||||
| chr19:50375913-50377866 | Common:110; Rare:2312 | ||||
| chr19:50383383-50384030 | Common:10; Rare:373 | ||||
| chr19:50383994-50384793 | Common:28; Rare:1284; Clinvar:11; Clinvar (benign):26 | ||||
| chr19:50398560-50399000 | Common:7; Rare:160; Clinvar:26; Clinvar (benign):15 | ||||
| chr19:50414860-50415140 | Common:2; Rare:82; Clinvar:17; Clinvar (benign):17 | ||||
| chr19:50415731-50416131 | Common:1; Rare:195; Clinvar:33; Clinvar (benign):23 | ||||
| chr19:50476151-50476565 | Common:3; Rare:612 | ||||
| chr19:50476535-50477170 | Common:1; Rare:397 | ||||
| chr19:50511070-50511750 | Common:33; Rare:1165 | ||||
| chr19:50568240-50568950 | Common:1; Rare:260 | ||||
| chr19:50639697-50640251 | Common:27; Rare:509 | ||||
| chr19:50649523-50650449 | Common:9; Rare:381 | ||||
| chr19:50657920-50658583 | Common:7; Rare:632 | ||||
| chr19:50658488-50659350 | Common:2; Rare:466 |