| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19202744-19203790 | Common:6; Rare:509 | ||||
| chr19:19320301-19321743 | Common:61; Rare:1998 | ||||
| chr19:19321837-19322237 | Common:4; Rare:97 | ||||
| chr19:19385222-19386166 | Common:4; Rare:1389 | ||||
| chr19:19405140-19406030 | Common:30; Rare:1121 | ||||
| chr19:19465170-19465780 | Common:3; Rare:165 | ||||
| chr19:19515936-19516600 | Common:4; Rare:983; Clinvar:5; Clinvar (pathogenic):6 | ||||
| chr19:19540364-19540764 | Rare:200 | ||||
| chr19:19618640-19618980 | Rare:283 | ||||
| chr19:19642906-19643504 | Common:4; Rare:237 | ||||
| chr19:19643540-19643930 | Common:18; Rare:306 | ||||
| chr19:19661843-19662389 | Common:5; Rare:328 | ||||
| chr19:19662321-19662721 | Common:3; Rare:63 | ||||
| chr19:19662801-19663201 | Common:5; Rare:153 | ||||
| chr19:19663119-19663934 | Rare:929 |