| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41310133-41310301 | Rare:72 | ||||
| chr19:41353780-41354115 | Common:2; Rare:109 | ||||
| chr19:41363794-41364000 | Common:1; Rare:75; Clinvar:1 | ||||
| chr19:41364080-41364178 | Common:1; Rare:28; Clinvar:2 | ||||
| chr19:41397318-41397859 | Common:11; Rare:169; Clinvar (benign):5 | ||||
| chr19:41860102-41860426 | Common:5; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41884142-41884444 | Rare:75 | ||||
| chr19:41959149-41959166 | Rare:5 | ||||
| chr19:42075805-42076191 | Rare:109 | ||||
| chr19:42132392-42132627 | Rare:53 | ||||
| chr19:42217671-42217874 | Rare:78 | ||||
| chr19:42220108-42220354 | Common:2; Rare:66 | ||||
| chr19:42254558-42254687 | Common:1; Rare:42 | ||||
| chr19:42302316-42302534 | Rare:62 | ||||
| chr19:42412395-42412434 | Rare:5 |