| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17405342-17405847 | Common:6; Rare:124 | ||||
| chr19:17859577-17859969 | Common:3; Rare:116 | ||||
| chr19:18152990-18153292 | Common:1; Rare:100 | ||||
| chr19:18173543-18173830 | Rare:55 | ||||
| chr19:18280097-18280446 | Common:4; Rare:130 | ||||
| chr19:18323043-18323351 | Common:3; Rare:101 | ||||
| chr19:18433385-18433613 | Common:1; Rare:74 | ||||
| chr19:18557760-18557890 | Common:2; Rare:35 | ||||
| chr19:18571679-18571906 | Common:3; Rare:103 | ||||
| chr19:18919339-18919744 | Common:2; Rare:144 | ||||
| chr19:18941233-18941531 | Common:4; Rare:74 | ||||
| chr19:19033475-19033653 | Common:2; Rare:55 | ||||
| chr19:19105720-19105823 | Common:1; Rare:34; Clinvar (pathogenic):1 | ||||
| chr19:19192103-19192268 | Common:1; Rare:52 | ||||
| chr19:19192614-19192969 | Common:2; Rare:85 |