| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49085086-49085530 | Common:3; Rare:172 | ||||
| chr19:49362375-49362477 | Rare:31 | ||||
| chr19:49451748-49452002 | Common:3; Rare:66 | ||||
| chr19:49453024-49453311 | Common:2; Rare:88 | ||||
| chr19:49453487-49453639 | Common:1; Rare:46 | ||||
| chr19:49496278-49496471 | Common:1; Rare:74 | ||||
| chr19:49513335-49513403 | Rare:14 | ||||
| chr19:49527858-49528038 | Common:3; Rare:57 | ||||
| chr19:49580528-49580644 | Rare:42 | ||||
| chr19:49641826-49642069 | Rare:70 | ||||
| chr19:49665739-49666029 | Common:3; Rare:137; Clinvar (pathogenic):1 | ||||
| chr19:49690978-49691142 | Rare:36 | ||||
| chr19:49850806-49851027 | Common:1; Rare:79 | ||||
| chr19:49851045-49851120 | Rare:31 | ||||
| chr19:49867539-49867633 | Common:2; Rare:33 |