| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41902073-41902342 | Rare:76 | ||||
| chr19:41903234-41903345 | Rare:24 | ||||
| chr19:41956905-41957131 | Rare:66 | ||||
| chr19:41959272-41959483 | Common:1; Rare:69 | ||||
| chr19:42075813-42076191 | Rare:105 | ||||
| chr19:42132416-42132627 | Rare:44 | ||||
| chr19:42217671-42217957 | Common:1; Rare:102 | ||||
| chr19:42220128-42220349 | Common:2; Rare:62 | ||||
| chr19:42302424-42302470 | Rare:12 | ||||
| chr19:42325414-42325675 | Rare:66 | ||||
| chr19:42512386-42512582 | Rare:55 | ||||
| chr19:42527363-42527515 | Rare:39 | ||||
| chr19:42528316-42528669 | Common:3; Rare:89; Clinvar:1 | ||||
| chr19:43527090-43527265 | Common:6; Rare:68; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr19:43619562-43619639 | Rare:31 |