| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126595143-126595370 | Common:5; Rare:102; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr5:126600856-126600993 | Common:1; Rare:65 | ||||
| chr5:126776931-126777225 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:127030509-127030764 | Common:2; Rare:61 | ||||
| chr5:127073449-127073544 | Common:3; Rare:29 | ||||
| chr5:127290700-127290893 | Rare:41 | ||||
| chr5:127517490-127517710 | Common:7; Rare:98 | ||||
| chr5:129094484-129094787 | Common:3; Rare:133 | ||||
| chr5:131165194-131165365 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr5:131170686-131171029 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr5:131635163-131635447 | Common:1; Rare:106 | ||||
| chr5:131796969-131797213 | Rare:67 | ||||
| chr5:132257517-132257732 | Common:7; Rare:52 | ||||
| chr5:132294081-132294202 | Rare:30 | ||||
| chr5:132294244-132294382 | Common:1; Rare:30 |