| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41219026-41219411 | Common:1; Rare:93 | ||||
| chr19:41262336-41262565 | Rare:44 | ||||
| chr19:41262827-41263240 | Common:3; Rare:69 | ||||
| chr19:41264997-41265109 | Common:1; Rare:20 | ||||
| chr19:41298333-41298612 | Common:1; Rare:46 | ||||
| chr19:41310086-41310303 | Rare:89 | ||||
| chr19:41353727-41354045 | Common:2; Rare:104 | ||||
| chr19:41363795-41363996 | Common:1; Rare:71; Clinvar:1 | ||||
| chr19:41364137-41364182 | Rare:13 | ||||
| chr19:41397332-41397604 | Common:4; Rare:71 | ||||
| chr19:41796553-41796607 | Rare:10 | ||||
| chr19:41860080-41860278 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:41861003-41861207 | Rare:66; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:41898191-41898491 | Common:2; Rare:81 | ||||
| chr19:42075816-42076199 | Rare:105 |