| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35745330-35745701 | Rare:113 | ||||
| chr19:35748244-35748674 | Common:3; Rare:121 | ||||
| chr19:35757467-35757559 | Common:1; Rare:19 | ||||
| chr19:35757629-35757717 | Rare:16 | ||||
| chr19:35757813-35758307 | Common:2; Rare:152 | ||||
| chr19:35758504-35758621 | Common:1; Rare:24 | ||||
| chr19:35775255-35775610 | Common:1; Rare:96 | ||||
| chr19:35845446-35845698 | Common:2; Rare:84; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:35900485-35900711 | Common:1; Rare:51 | ||||
| chr19:35994999-35995293 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35995412-35995488 | Rare:26; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:35995665-35995896 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr19:36008535-36008595 | Rare:30; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:36008699-36008958 | Rare:65; Clinvar (benign):1 | ||||
| chr19:36014169-36014609 | Common:2; Rare:118 |