| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48859324-48859502 | Rare:39 | ||||
| chr19:48872200-48872586 | Common:2; Rare:125 | ||||
| chr19:48896284-48896424 | Common:3; Rare:33 | ||||
| chr19:48899989-48900429 | Common:2; Rare:120 | ||||
| chr19:48918244-48918372 | Rare:24 | ||||
| chr19:48954594-48954921 | Common:1; Rare:116 | ||||
| chr19:48955153-48955352 | Common:1; Rare:47 | ||||
| chr19:48964974-48965483 | Common:1; Rare:129; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr19:48965681-48965781 | Rare:31 | ||||
| chr19:48993190-48993608 | Common:4; Rare:177; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993703-48993974 | Common:5; Rare:84 | ||||
| chr19:49031774-49031953 | Common:7; Rare:104 | ||||
| chr19:49085033-49085570 | Common:3; Rare:200 | ||||
| chr19:49085636-49085738 | Rare:41 | ||||
| chr19:49114271-49114370 | Rare:20 |