| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19385244-19386227 | Common:2; Rare:659 | ||||
| chr19:19405340-19405850 | Common:8; Rare:303 | ||||
| chr19:19464440-19464860 | Common:4; Rare:122 | ||||
| chr19:19514802-19515770 | Common:1; Rare:476 | ||||
| chr19:19516064-19516336 | Rare:441; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr19:19618644-19618927 | Rare:178 | ||||
| chr19:19627930-19628102 | Common:2; Rare:81 | ||||
| chr19:19628125-19628422 | Rare:211 | ||||
| chr19:19628428-19628860 | Rare:162 | ||||
| chr19:19643508-19643771 | Common:6; Rare:129 | ||||
| chr19:19663094-19663580 | Common:1; Rare:248 | ||||
| chr19:19663598-19663971 | Rare:161 | ||||
| chr19:19663980-19664220 | Common:2; Rare:95 | ||||
| chr19:19668571-19669055 | Common:7; Rare:320 | ||||
| chr19:19732961-19733319 | Common:5; Rare:185 |