| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45468515-45469002 | Common:2; Rare:103 | ||||
| chr19:45469259-45469534 | Rare:85 | ||||
| chr19:45470090-45470366 | Rare:60 | ||||
| chr19:45506814-45506959 | Common:1; Rare:44 | ||||
| chr19:45507369-45507511 | Rare:40 | ||||
| chr19:45584765-45585184 | Common:5; Rare:142; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45692378-45692695 | Common:1; Rare:72 | ||||
| chr19:46346938-46347098 | Common:3; Rare:50 | ||||
| chr19:46600885-46601108 | Common:2; Rare:92 | ||||
| chr19:46601226-46601416 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr19:46608181-46608513 | Common:1; Rare:72; Clinvar (benign):6 | ||||
| chr19:46717025-46717210 | Common:2; Rare:51 | ||||
| chr19:46787447-46787558 | Rare:32 | ||||
| chr19:47112150-47112583 | Common:1; Rare:144 | ||||
| chr19:47113104-47113467 | Common:2; Rare:94 |