| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127517495-127517724 | Common:7; Rare:101 | ||||
| chr5:129094460-129094772 | Common:3; Rare:129 | ||||
| chr5:129460096-129460470 | Common:5; Rare:104 | ||||
| chr5:131165146-131165393 | Common:3; Rare:98; Clinvar (benign):2 | ||||
| chr5:131170651-131171013 | Common:1; Rare:87; Clinvar (benign):2 | ||||
| chr5:131263889-131264139 | Common:1; Rare:98 | ||||
| chr5:131635153-131635717 | Common:1; Rare:190 | ||||
| chr5:131796928-131797227 | Rare:85 | ||||
| chr5:132257483-132257732 | Common:8; Rare:65 | ||||
| chr5:132369648-132369929 | Common:7; Rare:86; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:132556784-132557265 | Common:1; Rare:164; Clinvar:1 | ||||
| chr5:132737454-132737688 | Rare:82 | ||||
| chr5:132866440-132866698 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963286-132963382 | Rare:19 | ||||
| chr5:132963623-132963835 | Common:1; Rare:49 |