| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48445866-48446033 | Common:1; Rare:59 | ||||
| chr19:48619125-48619605 | Common:1; Rare:161 | ||||
| chr19:48811003-48811086 | Rare:32 | ||||
| chr19:48872218-48872474 | Common:2; Rare:95 | ||||
| chr19:48900005-48900389 | Common:1; Rare:111 | ||||
| chr19:48918773-48919080 | Common:3; Rare:109 | ||||
| chr19:48954724-48954936 | Rare:77 | ||||
| chr19:48965468-48965916 | Common:1; Rare:162; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993280-48993918 | Common:8; Rare:217; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:49085088-49085541 | Common:3; Rare:177 | ||||
| chr19:49157613-49157824 | Common:1; Rare:62; Clinvar:1 | ||||
| chr19:49451748-49452001 | Common:3; Rare:64 | ||||
| chr19:49453024-49453311 | Common:2; Rare:88 | ||||
| chr19:49453465-49453613 | Rare:45 | ||||
| chr19:49474152-49474271 | Common:1; Rare:25 |