| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103897702-103897984 | Common:2; Rare:62 | ||||
| chr10:103967762-103967891 | Rare:30 | ||||
| chr10:103986694-103986984 | Common:2; Rare:68 | ||||
| chr10:104035474-104035830 | Common:4; Rare:108 | ||||
| chr10:104035892-104036214 | Common:13; Rare:121 | ||||
| chr10:104036254-104036497 | Common:1; Rare:57; Clinvar (pathogenic):1 | ||||
| chr10:104039966-104040245 | Rare:61; Clinvar:2 | ||||
| chr10:104041065-104041326 | Common:2; Rare:75; Clinvar:3 | ||||
| chr10:104042375-104042447 | Rare:17; Clinvar:1 | ||||
| chr10:104043817-104043834 | Rare:2 | ||||
| chr10:104045813-104046052 | Rare:60 | ||||
| chr10:104046745-104046854 | Rare:25; Clinvar:1 | ||||
| chr10:104048577-104048607 | Common:1; Rare:6 | ||||
| chr10:104053870-104054156 | Rare:78; Clinvar:2 | ||||
| chr10:104062242-104062397 | Rare:44 |