| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44748039-44748196 | Rare:31 | ||||
| chr19:44748397-44748741 | Common:2; Rare:92 | ||||
| chr19:44757401-44757580 | Rare:40 | ||||
| chr19:44906506-44906651 | Rare:42 | ||||
| chr19:44955251-44955420 | Common:2; Rare:49 | ||||
| chr19:45091591-45091670 | Rare:16 | ||||
| chr19:45092823-45092948 | Common:1; Rare:39 | ||||
| chr19:45370552-45370799 | Common:2; Rare:73 | ||||
| chr19:45405020-45405177 | Rare:35 | ||||
| chr19:45406340-45406694 | Common:3; Rare:89 | ||||
| chr19:45423477-45423954 | Common:5; Rare:105; Clinvar (benign):1 | ||||
| chr19:45428762-45428921 | Rare:39 | ||||
| chr19:45450733-45451058 | Common:4; Rare:62 | ||||
| chr19:45467574-45467762 | Common:1; Rare:56 | ||||
| chr19:45468173-45468295 | Rare:30 |