| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40458007-40458900 | Common:12; Rare:514 | ||||
| chr19:40465098-40465498 | Rare:116 | ||||
| chr19:40465625-40466198 | Common:20; Rare:891 | ||||
| chr19:40530078-40530633 | Common:9; Rare:241 | ||||
| chr19:40570310-40571060 | Common:8; Rare:312; Clinvar (pathogenic):1 | ||||
| chr19:40576061-40576461 | Common:1; Rare:75 | ||||
| chr19:40576601-40577327 | Common:17; Rare:528 | ||||
| chr19:40580015-40580415 | Common:3; Rare:168 | ||||
| chr19:40594824-40595224 | Common:2; Rare:107 | ||||
| chr19:40596935-40597335 | Common:2; Rare:503 | ||||
| chr19:40598121-40598556 | Rare:403 | ||||
| chr19:40599422-40599826 | Common:3; Rare:250; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:40600950-40601490 | Rare:342; Clinvar:2 | ||||
| chr19:40601670-40602286 | Common:3; Rare:167 | ||||
| chr19:40605761-40606525 | Common:18; Rare:379; Clinvar (benign):11; Clinvar (pathogenic):1 |