| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42132402-42132627 | Rare:45 | ||||
| chr19:42217647-42217874 | Rare:87 | ||||
| chr19:42220108-42220349 | Common:2; Rare:66 | ||||
| chr19:42268488-42268570 | Rare:21 | ||||
| chr19:42269110-42269282 | Rare:42 | ||||
| chr19:42302417-42302499 | Rare:18 | ||||
| chr19:42407325-42407793 | Common:5; Rare:145 | ||||
| chr19:42412324-42412449 | Rare:25 | ||||
| chr19:42412494-42412833 | Common:1; Rare:54 | ||||
| chr19:42423526-42423753 | Common:4; Rare:81 | ||||
| chr19:42423927-42424308 | Common:1; Rare:90 | ||||
| chr19:42427326-42427510 | Rare:37 | ||||
| chr19:43527170-43527315 | Common:5; Rare:57; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575502-43575827 | Common:2; Rare:82 | ||||
| chr19:43580461-43580643 | Common:4; Rare:31 |