| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40417023-40417330 | Common:1; Rare:66 | ||||
| chr19:40420806-40420922 | Common:1; Rare:23 | ||||
| chr19:40420939-40421520 | Common:4; Rare:117 | ||||
| chr19:40425180-40425492 | Common:4; Rare:72 | ||||
| chr19:40433808-40434161 | Common:1; Rare:93 | ||||
| chr19:40435346-40435609 | Common:2; Rare:38 | ||||
| chr19:40605343-40605546 | Rare:51; Clinvar:1 | ||||
| chr19:40605586-40605763 | Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:40605877-40605955 | Common:4; Rare:12 | ||||
| chr19:40719033-40719264 | Rare:53 | ||||
| chr19:40777434-40777701 | Common:2; Rare:55 | ||||
| chr19:40798163-40798346 | Common:1; Rare:46 | ||||
| chr19:40810728-40810906 | Common:3; Rare:43 | ||||
| chr19:40811022-40811200 | Common:1; Rare:36 | ||||
| chr19:41263352-41263490 | Rare:28 |