| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126595192-126595348 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):8 | ||||
| chr5:126600881-126601054 | Common:1; Rare:83 | ||||
| chr5:127517508-127517764 | Common:5; Rare:106 | ||||
| chr5:129094443-129094879 | Common:3; Rare:191 | ||||
| chr5:131170692-131171006 | Common:1; Rare:66; Clinvar (benign):2 | ||||
| chr5:131635141-131635424 | Common:1; Rare:109 | ||||
| chr5:131796948-131797215 | Rare:75 | ||||
| chr5:132369559-132369943 | Common:9; Rare:122; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:132410742-132410982 | Rare:49 | ||||
| chr5:132490761-132491043 | Rare:74 | ||||
| chr5:132556885-132557045 | Rare:63; Clinvar:1 | ||||
| chr5:132830612-132830787 | Rare:48 | ||||
| chr5:132866293-132866745 | Common:4; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963584-132963737 | Rare:48 | ||||
| chr5:133051852-133052357 | Common:1; Rare:161 |