| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48810852-48811100 | Rare:80 | ||||
| chr19:48835824-48835958 | Common:1; Rare:41 | ||||
| chr19:48868282-48868691 | Rare:72 | ||||
| chr19:48872206-48872531 | Common:2; Rare:113 | ||||
| chr19:48918695-48919091 | Common:4; Rare:131 | ||||
| chr19:48954703-48954931 | Rare:83 | ||||
| chr19:48965229-48965616 | Rare:120; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48965681-48965937 | Common:1; Rare:94; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr19:48993234-48993540 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993553-48993914 | Common:5; Rare:94 | ||||
| chr19:49085088-49085588 | Common:3; Rare:192 | ||||
| chr19:49114079-49114416 | Common:4; Rare:90 | ||||
| chr19:49119112-49119270 | Rare:52 | ||||
| chr19:49155367-49155529 | Rare:28 | ||||
| chr19:49157632-49157878 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 |