| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40580419-40580655 | Rare:82 | ||||
| chr19:40601218-40601384 | Rare:53 | ||||
| chr19:40609573-40609754 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr19:40623576-40623612 | Rare:8 | ||||
| chr19:40715068-40715187 | Rare:33 | ||||
| chr19:40716876-40717024 | Common:1; Rare:49 | ||||
| chr19:40717166-40717358 | Common:1; Rare:57 | ||||
| chr19:40750411-40750913 | Common:6; Rare:126 | ||||
| chr19:40751033-40751311 | Common:3; Rare:87 | ||||
| chr19:40751775-40751894 | Rare:26 | ||||
| chr19:40777921-40778298 | Common:1; Rare:103 | ||||
| chr19:40991007-40991291 | Common:1; Rare:62 | ||||
| chr19:41193134-41193267 | Common:1; Rare:43 | ||||
| chr19:41219289-41219410 | Common:1; Rare:41 | ||||
| chr19:41262344-41262589 | Rare:43 |