| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32585910-32586410 | Common:13; Rare:314 | ||||
| chr5:33440591-33441108 | Common:13; Rare:263 | ||||
| chr5:33441090-33441870 | Common:7; Rare:246 | ||||
| chr5:34007997-34008272 | Common:4; Rare:195; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:34656159-34656478 | Common:6; Rare:157 | ||||
| chr5:34838950-34839550 | Common:9; Rare:255 | ||||
| chr5:34915214-34915355 | Rare:38 | ||||
| chr5:34915472-34915805 | Common:2; Rare:181 | ||||
| chr5:34929258-34929698 | Common:3; Rare:239 | ||||
| chr5:34929803-34930009 | Rare:101 | ||||
| chr5:35195178-35195342 | Rare:56 | ||||
| chr5:36151816-36152240 | Rare:232 | ||||
| chr5:36241624-36241991 | Common:8; Rare:235; Clinvar:2; Clinvar (benign):8 | ||||
| chr5:36242090-36242470 | Common:4; Rare:105; Clinvar (benign):2 | ||||
| chr5:36876642-36876915 | Common:2; Rare:153; Clinvar:2; Clinvar (benign):2 |