| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192619-19192998 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr19:19320480-19320850 | Common:4; Rare:133 | ||||
| chr19:19516119-19516244 | Rare:74 | ||||
| chr19:19821708-19821873 | Common:1; Rare:54 | ||||
| chr19:19900757-19900958 | Rare:56 | ||||
| chr19:32405560-32405770 | Rare:85 | ||||
| chr19:32971885-32972280 | Common:4; Rare:115 | ||||
| chr19:34254534-34254601 | Rare:18 | ||||
| chr19:34365086-34365258 | Common:1; Rare:75 | ||||
| chr19:34428319-34428435 | Rare:50 | ||||
| chr19:34677546-34677758 | Common:5; Rare:61 | ||||
| chr19:35000176-35000481 | Common:4; Rare:74 | ||||
| chr19:35155155-35155230 | Rare:15 | ||||
| chr19:35545505-35545698 | Common:4; Rare:60 | ||||
| chr19:35628748-35629113 | Common:4; Rare:111 |