| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41363773-41364013 | Common:1; Rare:83; Clinvar:1 | ||||
| chr19:41364117-41364311 | Rare:61; Clinvar:1 | ||||
| chr19:41376683-41376766 | Rare:31 | ||||
| chr19:41397321-41397604 | Common:4; Rare:75 | ||||
| chr19:41750729-41751104 | Rare:61 | ||||
| chr19:41755308-41755705 | Common:2; Rare:87 | ||||
| chr19:41860139-41860506 | Common:5; Rare:136; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41884140-41884458 | Rare:83 | ||||
| chr19:42075805-42076199 | Rare:112 | ||||
| chr19:42132426-42132660 | Rare:47 | ||||
| chr19:42217661-42217874 | Rare:82 | ||||
| chr19:42220112-42220349 | Common:2; Rare:66 | ||||
| chr19:42232671-42232792 | Common:1; Rare:22 | ||||
| chr19:42302306-42302414 | Rare:37 | ||||
| chr19:42302422-42302498 | Rare:16 |