| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18571656-18571900 | Common:2; Rare:104 | ||||
| chr19:18588579-18588872 | Common:4; Rare:70 | ||||
| chr19:18683501-18683699 | Common:1; Rare:68 | ||||
| chr19:18919345-18919740 | Common:2; Rare:139 | ||||
| chr19:18941239-18941428 | Common:3; Rare:46 | ||||
| chr19:19033452-19033653 | Common:2; Rare:68 | ||||
| chr19:19033803-19033853 | Rare:14 | ||||
| chr19:19105711-19105852 | Common:1; Rare:47; Clinvar (pathogenic):1 | ||||
| chr19:19192113-19192245 | Common:1; Rare:42 | ||||
| chr19:19192563-19192991 | Common:2; Rare:112 | ||||
| chr19:19320471-19320874 | Common:4; Rare:153 | ||||
| chr19:19516157-19516331 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19668511-19668792 | Rare:65 | ||||
| chr19:19821637-19821905 | Common:1; Rare:90 | ||||
| chr19:19900763-19900991 | Common:1; Rare:67 |