| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:33868834-33869360 | Common:10; Rare:181 | ||||
| chr19:33884120-33884540 | Common:7; Rare:74 | ||||
| chr19:33905240-33905710 | Rare:103 | ||||
| chr19:33905932-33906205 | Common:3; Rare:150 | ||||
| chr19:33906280-33906500 | Rare:93 | ||||
| chr19:34134295-34134669 | Common:7; Rare:202 | ||||
| chr19:34270061-34270522 | Common:1; Rare:196 | ||||
| chr19:34310624-34310907 | Common:1; Rare:104 | ||||
| chr19:34377562-34377779 | Common:2; Rare:58; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:34859820-34860506 | Common:22; Rare:305 | ||||
| chr19:34921244-34921393 | Rare:23 | ||||
| chr19:35003320-35003647 | Rare:210 | ||||
| chr19:35006293-35006870 | Common:1; Rare:204 | ||||
| chr19:35066840-35067110 | Common:6; Rare:105 | ||||
| chr19:35111001-35111735 | Common:21; Rare:264 |