| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12806433-12806674 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:12806767-12806837 | Rare:31; Clinvar (pathogenic):1 | ||||
| chr19:12833865-12833953 | Rare:16 | ||||
| chr19:12881381-12881591 | Rare:41 | ||||
| chr19:12890751-12891240 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:12919180-12919521 | Common:3; Rare:168 | ||||
| chr19:12932966-12933304 | Common:1; Rare:63 | ||||
| chr19:12933645-12933902 | Common:1; Rare:78 | ||||
| chr19:12938184-12938646 | Common:5; Rare:163 | ||||
| chr19:12945716-12946015 | Common:2; Rare:105 | ||||
| chr19:12946119-12946412 | Rare:72 | ||||
| chr19:12956994-12957335 | Common:1; Rare:112 | ||||
| chr19:12965502-12965578 | Rare:16 | ||||
| chr19:12995489-12995571 | Rare:26 | ||||
| chr19:13116157-13116301 | Rare:57 |