| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39402985-39403056 | Rare:12 | ||||
| chr19:39403749-39404197 | Common:1; Rare:94 | ||||
| chr19:39409505-39409637 | Common:1; Rare:34 | ||||
| chr19:39409646-39409854 | Common:1; Rare:52 | ||||
| chr19:39410047-39410236 | Rare:38 | ||||
| chr19:39411179-39411363 | Rare:44 | ||||
| chr19:39444347-39444636 | Common:1; Rare:46 | ||||
| chr19:39444984-39445040 | Rare:13 | ||||
| chr19:39507102-39507395 | Rare:132; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:39558438-39558538 | Common:1; Rare:15 | ||||
| chr19:39679157-39679382 | Common:1; Rare:37 | ||||
| chr19:39679401-39679681 | Common:4; Rare:53 | ||||
| chr19:39705991-39706081 | Rare:34 | ||||
| chr19:39795118-39795249 | Rare:29 | ||||
| chr19:39818831-39818984 | Common:1; Rare:27 |