| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45038951-45039104 | Rare:54 | ||||
| chr19:45079176-45079297 | Rare:33 | ||||
| chr19:45091583-45091764 | Common:1; Rare:47 | ||||
| chr19:45370536-45370782 | Common:2; Rare:79 | ||||
| chr19:45406340-45406649 | Common:1; Rare:67 | ||||
| chr19:45423402-45423779 | Common:3; Rare:77; Clinvar (benign):2 | ||||
| chr19:45423837-45423889 | Common:1; Rare:16 | ||||
| chr19:45423892-45424032 | Common:1; Rare:23 | ||||
| chr19:45450733-45451031 | Common:4; Rare:56 | ||||
| chr19:45469203-45469476 | Rare:87 | ||||
| chr19:45507228-45507528 | Common:1; Rare:83 | ||||
| chr19:45584779-45585072 | Common:4; Rare:106; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45639356-45639482 | Common:1; Rare:36 | ||||
| chr19:45692365-45692722 | Common:1; Rare:86 | ||||
| chr19:45730857-45731137 | Common:1; Rare:63 |