| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:8444859-8445109 | Common:2; Rare:116; Clinvar (benign):1 | ||||
| chr19:8463490-8463504 | Rare:1 | ||||
| chr19:8513678-8513708 | Rare:2 | ||||
| chr19:8514045-8514232 | Common:2; Rare:56 | ||||
| chr19:8526342-8526491 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr19:8832163-8832367 | Common:2; Rare:74 | ||||
| chr19:9140319-9140437 | Rare:35 | ||||
| chr19:9362695-9363046 | Common:1; Rare:88 | ||||
| chr19:9435475-9435641 | Common:1; Rare:63 | ||||
| chr19:9538579-9538887 | Common:1; Rare:90 | ||||
| chr19:9621157-9621619 | Common:4; Rare:143 | ||||
| chr19:9675050-9675386 | Common:1; Rare:110 | ||||
| chr19:9818800-9818864 | Rare:24 | ||||
| chr19:9819038-9819123 | Rare:26 | ||||
| chr19:9827805-9828000 | Common:1; Rare:69 |