| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126595183-126595337 | Common:3; Rare:73; Clinvar:4; Clinvar (benign):8 | ||||
| chr5:127030545-127030732 | Common:2; Rare:42 | ||||
| chr5:127517480-127517699 | Common:7; Rare:98 | ||||
| chr5:129460106-129460314 | Common:4; Rare:32 | ||||
| chr5:131170692-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:131635177-131635315 | Common:1; Rare:62 | ||||
| chr5:131796969-131797202 | Rare:66 | ||||
| chr5:132257476-132257727 | Common:8; Rare:65 | ||||
| chr5:132369598-132369964 | Common:8; Rare:120; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:132410601-132410951 | Common:1; Rare:67 | ||||
| chr5:132490774-132491020 | Rare:64 | ||||
| chr5:132556829-132556997 | Common:1; Rare:58; Clinvar:1 | ||||
| chr5:132737506-132737684 | Rare:53 | ||||
| chr5:132866501-132866688 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963286-132963393 | Rare:22 |