| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124748758-124748998 | Common:2; Rare:54 | ||||
| chr5:126595192-126595337 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):8 | ||||
| chr5:127030545-127030768 | Common:2; Rare:51 | ||||
| chr5:129094471-129094767 | Common:3; Rare:120 | ||||
| chr5:131170708-131170996 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr5:131635160-131635472 | Common:1; Rare:118 | ||||
| chr5:131796969-131797215 | Rare:67 | ||||
| chr5:132369589-132369719 | Common:2; Rare:36 | ||||
| chr5:132490754-132490994 | Rare:56 | ||||
| chr5:132866329-132866690 | Common:1; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051856-133052113 | Rare:97 | ||||
| chr5:133968580-133968687 | Rare:47 | ||||
| chr5:134004649-134004834 | Common:1; Rare:69 | ||||
| chr5:134004935-134005111 | Rare:37 | ||||
| chr5:134371031-134371184 | Common:1; Rare:39 |