| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32063780-32064049 | Common:3; Rare:299; Clinvar:14; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr2:32064058-32064466 | Rare:277; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr2:32165592-32165939 | Common:4; Rare:336 | ||||
| chr2:32277737-32277988 | Common:2; Rare:115 | ||||
| chr2:32278030-32278475 | Common:1; Rare:179 | ||||
| chr2:32356427-32356769 | Common:1; Rare:114 | ||||
| chr2:32356783-32357285 | Common:15; Rare:488 | ||||
| chr2:32357382-32357572 | Rare:44 | ||||
| chr2:32627899-32628258 | Rare:200 | ||||
| chr2:32946754-32947194 | Common:8; Rare:324 | ||||
| chr2:32947206-32947505 | Common:4; Rare:71 | ||||
| chr2:33291290-33291720 | Common:1; Rare:72 | ||||
| chr2:33599189-33599673 | Common:3; Rare:388 | ||||
| chr2:36355449-36357242 | Common:17; Rare:1198 | ||||
| chr2:36597550-36597946 | Common:6; Rare:231 |