| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39970918-39971196 | Common:4; Rare:76 | ||||
| chr19:40056147-40056260 | Rare:15 | ||||
| chr19:40348364-40348715 | Common:4; Rare:110 | ||||
| chr19:40576708-40576893 | Common:2; Rare:53 | ||||
| chr19:40751068-40751239 | Common:1; Rare:47 | ||||
| chr19:41219115-41219411 | Common:1; Rare:79 | ||||
| chr19:41364137-41364317 | Rare:55 | ||||
| chr19:41860080-41860278 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:43670135-43670306 | Common:2; Rare:41 | ||||
| chr19:43754901-43755112 | Common:3; Rare:73 | ||||
| chr19:43827249-43827424 | Common:2; Rare:37 | ||||
| chr19:44002794-44002986 | Common:4; Rare:49 | ||||
| chr19:44025225-44025410 | Common:1; Rare:41 | ||||
| chr19:44071946-44072164 | Common:1; Rare:54 | ||||
| chr19:44141521-44141588 | Rare:9 |