| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192104-19192274 | Common:1; Rare:52 | ||||
| chr19:19192601-19192991 | Common:2; Rare:96 | ||||
| chr19:19203300-19203539 | Common:1; Rare:65 | ||||
| chr19:19320474-19320850 | Common:4; Rare:138 | ||||
| chr19:19516155-19516331 | Rare:105; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19528158-19528432 | Rare:58 | ||||
| chr19:19643582-19643713 | Common:3; Rare:39 | ||||
| chr19:19821700-19821873 | Common:1; Rare:58 | ||||
| chr19:19900763-19900953 | Rare:54 | ||||
| chr19:21082018-21082280 | Rare:58 | ||||
| chr19:21141855-21142077 | Rare:61 | ||||
| chr19:21396879-21397167 | Rare:70 | ||||
| chr19:22052368-22052450 | Rare:9 | ||||
| chr19:24033311-24033573 | Common:7; Rare:57 | ||||
| chr19:29213138-29213351 | Common:3; Rare:68 |