| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37932324-37932428 | Rare:25 | ||||
| chr19:38224140-38224430 | Common:1; Rare:85 | ||||
| chr19:38228073-38228473 | Common:3; Rare:71 | ||||
| chr19:38229655-38229917 | Common:1; Rare:66 | ||||
| chr19:38287832-38288049 | Common:1; Rare:53; Clinvar (pathogenic):1 | ||||
| chr19:38315759-38316129 | Rare:121 | ||||
| chr19:38335590-38335960 | Common:2; Rare:73 | ||||
| chr19:38336290-38336465 | Common:2; Rare:39 | ||||
| chr19:38336829-38337229 | Common:11; Rare:139 | ||||
| chr19:38374343-38374796 | Rare:163 | ||||
| chr19:38387678-38387788 | Rare:34 | ||||
| chr19:38388624-38389362 | Common:1; Rare:205 | ||||
| chr19:38389580-38389870 | Rare:43 | ||||
| chr19:38402914-38403207 | Common:5; Rare:105 | ||||
| chr19:38433351-38433901 | Common:10; Rare:254; Clinvar:1; Clinvar (benign):6 |