| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45370552-45370799 | Common:2; Rare:73 | ||||
| chr19:45406363-45406649 | Common:1; Rare:62 | ||||
| chr19:45507228-45507499 | Common:1; Rare:68 | ||||
| chr19:45692438-45692691 | Common:1; Rare:56 | ||||
| chr19:45730860-45731011 | Common:1; Rare:31 | ||||
| chr19:45769375-45769639 | Common:1; Rare:122 | ||||
| chr19:46023051-46023212 | Common:2; Rare:35 | ||||
| chr19:46296829-46297062 | Common:4; Rare:85 | ||||
| chr19:46298143-46298443 | Common:5; Rare:75 | ||||
| chr19:46346927-46347156 | Common:3; Rare:78 | ||||
| chr19:46413552-46413743 | Common:1; Rare:62 | ||||
| chr19:46471480-46471640 | Common:5; Rare:60 | ||||
| chr19:46600908-46601411 | Common:5; Rare:174; Clinvar (benign):1 | ||||
| chr19:46745750-46746066 | Common:4; Rare:64 | ||||
| chr19:46746807-46746904 | Rare:13 |