| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19516167-19516295 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821700-19821873 | Common:1; Rare:58 | ||||
| chr19:19900807-19900953 | Rare:34 | ||||
| chr19:21358836-21359037 | Common:3; Rare:54 | ||||
| chr19:21396951-21397128 | Rare:36 | ||||
| chr19:24033311-24033497 | Common:6; Rare:40 | ||||
| chr19:29213138-29213282 | Common:2; Rare:47 | ||||
| chr19:29665253-29665484 | Common:4; Rare:84 | ||||
| chr19:29715193-29715305 | Common:1; Rare:44 | ||||
| chr19:31349217-31349512 | Common:4; Rare:100 | ||||
| chr19:32971876-32972313 | Common:5; Rare:128 | ||||
| chr19:33081093-33081233 | Common:1; Rare:54 | ||||
| chr19:33373553-33373812 | Common:2; Rare:87 | ||||
| chr19:33521765-33521931 | Rare:53; Clinvar:3 | ||||
| chr19:34172420-34172560 | Rare:61 |