| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18323034-18323297 | Common:3; Rare:82 | ||||
| chr19:18557668-18557911 | Common:5; Rare:62 | ||||
| chr19:18919316-18919740 | Common:2; Rare:162 | ||||
| chr19:19033473-19033653 | Common:2; Rare:57 | ||||
| chr19:19033798-19033916 | Common:1; Rare:31 | ||||
| chr19:19192110-19192212 | Common:1; Rare:35 | ||||
| chr19:19192594-19192920 | Common:2; Rare:84 | ||||
| chr19:19320522-19320850 | Common:4; Rare:113 | ||||
| chr19:19516167-19516331 | Rare:95; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821652-19821866 | Common:1; Rare:70 | ||||
| chr19:29212904-29213213 | Common:3; Rare:83 | ||||
| chr19:29665241-29665496 | Common:4; Rare:90 | ||||
| chr19:29715015-29715291 | Common:1; Rare:98 | ||||
| chr19:32675114-32675439 | Common:4; Rare:107 | ||||
| chr19:32691664-32691821 | Rare:41 |