| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45730869-45731073 | Common:1; Rare:45 | ||||
| chr19:45769153-45769363 | Rare:67 | ||||
| chr19:46471484-46471608 | Common:5; Rare:50 | ||||
| chr19:46600913-46601420 | Common:5; Rare:175; Clinvar (benign):1 | ||||
| chr19:46746044-46746061 | Rare:3 | ||||
| chr19:46788412-46788558 | Rare:36 | ||||
| chr19:47113789-47113964 | Common:1; Rare:35 | ||||
| chr19:47130802-47130964 | Common:1; Rare:69 | ||||
| chr19:47256472-47256583 | Rare:42 | ||||
| chr19:47349045-47349352 | Common:1; Rare:90 | ||||
| chr19:47484191-47484302 | Common:1; Rare:35 | ||||
| chr19:47512764-47512866 | Rare:22 | ||||
| chr19:47514841-47514971 | Rare:41 | ||||
| chr19:48170275-48170709 | Common:2; Rare:116 | ||||
| chr19:48321317-48321495 | Common:1; Rare:57 |