| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131796905-131797221 | Rare:90 | ||||
| chr5:132369671-132369936 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:132556836-132557039 | Common:1; Rare:74; Clinvar:1 | ||||
| chr5:132737425-132737732 | Rare:107 | ||||
| chr5:132866470-132866713 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133026537-133026722 | Common:3; Rare:44 | ||||
| chr5:133051862-133052357 | Common:1; Rare:156 | ||||
| chr5:133968582-133968688 | Rare:47 | ||||
| chr5:134004521-134004855 | Common:1; Rare:113 | ||||
| chr5:134004913-134005064 | Rare:32 | ||||
| chr5:134225537-134225622 | Common:1; Rare:30 | ||||
| chr5:134225952-134226447 | Common:1; Rare:158 | ||||
| chr5:134367146-134367281 | Common:1; Rare:42 | ||||
| chr5:134371023-134371637 | Common:5; Rare:205 | ||||
| chr5:134411755-134412008 | Rare:94 |