| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132737506-132737686 | Rare:54 | ||||
| chr5:132866408-132866681 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chr5:133051862-133052185 | Rare:111 | ||||
| chr5:133968573-133968738 | Rare:65 | ||||
| chr5:134004649-134004850 | Common:1; Rare:74 | ||||
| chr5:134004928-134005082 | Rare:31 | ||||
| chr5:134371027-134371184 | Common:1; Rare:40 | ||||
| chr5:134632768-134632933 | Rare:32 | ||||
| chr5:134648726-134648816 | Rare:20 | ||||
| chr5:134758559-134758813 | Common:1; Rare:88 | ||||
| chr5:134845832-134846094 | Rare:118 | ||||
| chr5:134874236-134874423 | Common:1; Rare:90 | ||||
| chr5:135399105-135399329 | Rare:61 | ||||
| chr5:138033062-138033302 | Common:1; Rare:71 | ||||
| chr5:138178941-138179127 | Common:2; Rare:41 |