| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40993469-40993549 | Rare:17 | ||||
| chr19:42396907-42397156 | Common:1; Rare:58 | ||||
| chr19:44725142-44725471 | Common:5; Rare:82 | ||||
| chr19:44737350-44737675 | Common:1; Rare:55 | ||||
| chr19:44924375-44924605 | Common:3; Rare:45 | ||||
| chr19:44926668-44927020 | Common:2; Rare:75 | ||||
| chr19:45245359-45245648 | Common:2; Rare:75 | ||||
| chr19:46350742-46350872 | Common:2; Rare:25 | ||||
| chr19:46860778-46861142 | Common:3; Rare:116 | ||||
| chr19:48908885-48909066 | Rare:36 | ||||
| chr19:48962370-48962578 | Common:2; Rare:50 | ||||
| chr19:48966803-48967093 | Common:2; Rare:47; Clinvar:1 | ||||
| chr19:49491486-49491794 | Common:1; Rare:101 | ||||
| chr19:49829859-49830165 | Common:1; Rare:114; Clinvar:6; Clinvar (benign):4 | ||||
| chr19:51140567-51140712 | Common:1; Rare:22 |