| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32277765-32277986 | Common:1; Rare:55 | ||||
| chr2:32627924-32628297 | Rare:107 | ||||
| chr2:33134082-33134747 | Common:3; Rare:146 | ||||
| chr2:33599202-33599415 | Rare:82 | ||||
| chr2:37084267-37084561 | Common:4; Rare:110 | ||||
| chr2:37212382-37212553 | Rare:39 | ||||
| chr2:37213862-37214071 | Rare:54 | ||||
| chr2:37231451-37231726 | Common:5; Rare:142; Clinvar (benign):4 | ||||
| chr2:37231825-37232117 | Common:2; Rare:77 | ||||
| chr2:37243753-37243925 | Rare:59; Clinvar (benign):2 | ||||
| chr2:37274573-37274843 | Common:1; Rare:70 | ||||
| chr2:37324695-37324950 | Common:1; Rare:100 | ||||
| chr2:37671514-37671773 | Common:2; Rare:106 | ||||
| chr2:38075956-38075969 | Rare:2 | ||||
| chr2:38076143-38076288 | Rare:37 |