| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2269753-2269856 | Common:2; Rare:43 | ||||
| chr19:2328575-2328703 | Common:2; Rare:64 | ||||
| chr19:2427868-2428092 | Common:4; Rare:74 | ||||
| chr19:2785264-2785554 | Common:5; Rare:88 | ||||
| chr19:2841203-2841548 | Common:2; Rare:109 | ||||
| chr19:3982986-3983221 | Common:2; Rare:86; Clinvar (benign):1 | ||||
| chr19:4471966-4472321 | Common:5; Rare:129 | ||||
| chr19:4867665-4867859 | Common:2; Rare:56 | ||||
| chr19:5293213-5293428 | Common:1; Rare:97 | ||||
| chr19:5622737-5623195 | Common:5; Rare:180 | ||||
| chr19:5978078-5978383 | Common:3; Rare:113 | ||||
| chr19:7395023-7395197 | Common:4; Rare:54 | ||||
| chr19:7629535-7629845 | Common:5; Rare:109; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7943644-7943990 | Rare:90 | ||||
| chr19:8005525-8005825 | Common:1; Rare:107 |