| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58408425-58408720 | Common:4; Rare:97 | ||||
| chr19:58451486-58451660 | Common:2; Rare:72 | ||||
| chr19:58476032-58476184 | Rare:54 | ||||
| chr19:58499206-58499637 | Common:2; Rare:153; Clinvar:6; Clinvar (benign):1 | ||||
| chr19:58519534-58520035 | Rare:122 | ||||
| chr19:58543975-58544121 | Rare:39 | ||||
| chr19:58544178-58544537 | Common:3; Rare:162 | ||||
| chr19:58544554-58544799 | Rare:100 | ||||
| chr19:58557644-58557802 | Common:2; Rare:27 | ||||
| chr19:58558318-58558720 | Rare:132 | ||||
| chr19:58558890-58559158 | Common:1; Rare:85 | ||||
| chr19:58564150-58564184 | Rare:10 | ||||
| chr19:58564363-58564642 | Common:1; Rare:54 | ||||
| chr19:58573307-58573764 | Common:4; Rare:116 | ||||
| chr2:264546-265010 | Common:4; Rare:183 |