| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134004545-134004869 | Common:1; Rare:106 | ||||
| chr5:134226061-134226410 | Common:1; Rare:105 | ||||
| chr5:134411859-134412008 | Rare:47 | ||||
| chr5:134648729-134648878 | Rare:41 | ||||
| chr5:135399164-135399286 | Rare:29 | ||||
| chr5:138178953-138179187 | Common:2; Rare:47 | ||||
| chr5:138543110-138543283 | Common:1; Rare:51 | ||||
| chr5:138753236-138753481 | Common:2; Rare:85 | ||||
| chr5:139482756-139482895 | Rare:21 | ||||
| chr5:139561702-139561811 | Rare:42 | ||||
| chr5:140564308-140564481 | Common:1; Rare:47 | ||||
| chr5:140647594-140647880 | Common:5; Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691257-140691644 | Common:2; Rare:137; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320725-141320886 | Common:2; Rare:51 | ||||
| chr5:141636825-141636997 | Common:1; Rare:68 |