| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18001020-18001296 | Common:2; Rare:69 | ||||
| chr19:18008002-18008171 | Common:5; Rare:62 | ||||
| chr19:18086685-18087105 | Common:3; Rare:122; Clinvar (benign):2 | ||||
| chr19:18097752-18097863 | Rare:21 | ||||
| chr19:18097954-18098269 | Rare:47 | ||||
| chr19:18098786-18099140 | Rare:57 | ||||
| chr19:18099158-18099719 | Common:1; Rare:112 | ||||
| chr19:18109966-18110134 | Common:2; Rare:35 | ||||
| chr19:18110370-18110598 | Common:3; Rare:33 | ||||
| chr19:18152398-18152681 | Rare:72 | ||||
| chr19:18152891-18153367 | Common:2; Rare:138 | ||||
| chr19:18173503-18173894 | Common:3; Rare:78 | ||||
| chr19:18174102-18174207 | Rare:24 | ||||
| chr19:18174344-18174545 | Rare:41 | ||||
| chr19:18192700-18193343 | Common:4; Rare:181; Clinvar:1 |