| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178523046-178523239 | Rare:58 | ||||
| chr2:188990093-188990361 | Rare:78; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr2:188996122-188996494 | Common:12; Rare:80; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188997162-188997390 | Common:5; Rare:59; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr2:189001421-189001585 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr2:189004061-189004364 | Rare:90; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):19 | ||||
| chr2:191209471-191209609 | Common:2; Rare:15 | ||||
| chr2:207239419-207239593 | Rare:26 | ||||
| chr2:227818069-227818165 | Common:2; Rare:12 | ||||
| chr2:227818172-227818472 | Common:2; Rare:46 | ||||
| chr2:231514362-231514577 | Common:5; Rare:85 | ||||
| chr2:237353339-237353654 | Common:3; Rare:68; Clinvar:4; Clinvar (benign):2 | ||||
| chr20:3804534-3804860 | Common:2; Rare:100 | ||||
| chr20:19757489-19757690 | Common:3; Rare:59 | ||||
| chr20:19757929-19758282 | Common:5; Rare:122 |