| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41262396-41262598 | Rare:35 | ||||
| chr19:41264952-41265113 | Common:2; Rare:36 | ||||
| chr19:41310144-41310272 | Rare:54 | ||||
| chr19:41364137-41364180 | Rare:12 | ||||
| chr19:41397332-41397604 | Common:4; Rare:71 | ||||
| chr19:41860080-41860285 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:42075811-42076191 | Rare:106 | ||||
| chr19:42220128-42220358 | Common:2; Rare:62 | ||||
| chr19:42302310-42302503 | Rare:55 | ||||
| chr19:42423543-42423753 | Common:4; Rare:74 | ||||
| chr19:42442840-42443042 | Common:3; Rare:36 | ||||
| chr19:42528422-42528593 | Common:2; Rare:41 | ||||
| chr19:43465551-43465829 | Common:1; Rare:87 | ||||
| chr19:43575478-43575818 | Common:2; Rare:89 | ||||
| chr19:43596045-43596433 | Common:3; Rare:121 |