| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132866457-132866694 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963331-132963393 | Rare:18 | ||||
| chr5:132963603-132963745 | Rare:44 | ||||
| chr5:133026523-133026754 | Common:4; Rare:51 | ||||
| chr5:133051862-133052216 | Rare:119 | ||||
| chr5:133968553-133968703 | Rare:68 | ||||
| chr5:134004535-134004850 | Common:1; Rare:101 | ||||
| chr5:134004905-134005010 | Rare:22 | ||||
| chr5:134226061-134226407 | Common:1; Rare:105 | ||||
| chr5:134371027-134371195 | Common:1; Rare:42 | ||||
| chr5:134648685-134648850 | Rare:50 | ||||
| chr5:134738319-134738615 | Rare:108 | ||||
| chr5:134758619-134758842 | Common:2; Rare:71 | ||||
| chr5:134845824-134846121 | Rare:133 | ||||
| chr5:134874282-134874423 | Common:1; Rare:74 |