| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47112151-47112367 | Rare:65 | ||||
| chr19:47112505-47112683 | Common:2; Rare:51 | ||||
| chr19:47256440-47256571 | Rare:44 | ||||
| chr19:47349053-47349420 | Common:1; Rare:107 | ||||
| chr19:47484261-47484307 | Rare:12 | ||||
| chr19:47778420-47778811 | Common:3; Rare:135 | ||||
| chr19:48170259-48170383 | Common:1; Rare:48 | ||||
| chr19:48255843-48255935 | Common:5; Rare:15 | ||||
| chr19:48391435-48391476 | Rare:11 | ||||
| chr19:48445890-48446005 | Rare:44 | ||||
| chr19:48619139-48619464 | Common:1; Rare:107 | ||||
| chr19:48810988-48811224 | Rare:71 | ||||
| chr19:48900157-48900367 | Common:1; Rare:68 | ||||
| chr19:48965236-48965609 | Rare:115; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993253-48993905 | Common:8; Rare:225; Clinvar:3; Clinvar (benign):2 |