| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58327235-58327342 | Rare:25 | ||||
| chr19:58347576-58347780 | Common:8; Rare:97 | ||||
| chr19:58408452-58408660 | Common:2; Rare:65 | ||||
| chr19:58499247-58499538 | Common:1; Rare:88; Clinvar:1 | ||||
| chr19:58554239-58554409 | Rare:37 | ||||
| chr19:58554931-58555183 | Common:1; Rare:85 | ||||
| chr19:58558906-58559150 | Common:1; Rare:75 | ||||
| chr2:677358-677564 | Common:1; Rare:87 | ||||
| chr2:1744412-1744638 | Common:1; Rare:75 | ||||
| chr2:3377785-3377953 | Rare:46 | ||||
| chr2:3379608-3379728 | Common:1; Rare:39 | ||||
| chr2:3519477-3519636 | Common:2; Rare:54 | ||||
| chr2:3558230-3558735 | Common:6; Rare:183 | ||||
| chr2:3575098-3575448 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:8837581-8837738 | Common:1; Rare:57 |