| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45038966-45039094 | Rare:42 | ||||
| chr19:45370550-45370723 | Common:1; Rare:50 | ||||
| chr19:45406340-45406682 | Common:2; Rare:84 | ||||
| chr19:45423477-45423676 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr19:45423837-45424012 | Common:2; Rare:38 | ||||
| chr19:45467911-45468027 | Rare:41 | ||||
| chr19:45584763-45585093 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45730869-45731189 | Common:1; Rare:71 | ||||
| chr19:46346941-46347119 | Common:3; Rare:54 | ||||
| chr19:46601186-46601394 | Common:3; Rare:59 | ||||
| chr19:46745969-46746071 | Common:3; Rare:27 | ||||
| chr19:46787282-46787525 | Common:1; Rare:71 | ||||
| chr19:46850245-46850384 | Rare:20 | ||||
| chr19:47112166-47112326 | Rare:49 | ||||
| chr19:47256472-47256577 | Rare:39 |