| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45075405-45075701 | Common:1; Rare:66 | ||||
| chr19:45767403-45767612 | Rare:60 | ||||
| chr19:45852363-45852521 | Rare:35 | ||||
| chr19:45885335-45885589 | Rare:88 | ||||
| chr19:46860842-46861148 | Common:3; Rare:97 | ||||
| chr19:47069324-47069610 | Common:3; Rare:87 | ||||
| chr19:47489722-47489916 | Rare:47 | ||||
| chr19:47503426-47503696 | Common:1; Rare:74 | ||||
| chr19:47730211-47730550 | Common:1; Rare:58 | ||||
| chr19:48873021-48873413 | Common:4; Rare:93 | ||||
| chr19:48920892-48921318 | Common:6; Rare:109 | ||||
| chr19:48966264-48966545 | Rare:92; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:49103732-49103918 | Rare:60 | ||||
| chr19:49635504-49635848 | Rare:117; Clinvar:4; Clinvar (benign):3 | ||||
| chr19:49636673-49636962 | Common:4; Rare:101; Clinvar:2; Clinvar (benign):6 |