| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128537494-128537650 | Rare:127; Clinvar:9; Clinvar (benign):16 | ||||
| chr5:128538210-128538570 | Common:9; Rare:94 | ||||
| chr5:129094443-129094767 | Common:3; Rare:132 | ||||
| chr5:129459920-129460400 | Common:6; Rare:110 | ||||
| chr5:131165193-131165419 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr5:131170612-131171022 | Common:1; Rare:92; Clinvar (benign):2 | ||||
| chr5:131263778-131264302 | Common:2; Rare:183 | ||||
| chr5:131634652-131634856 | Rare:40 | ||||
| chr5:131635159-131635757 | Common:1; Rare:194 | ||||
| chr5:131796968-131797291 | Rare:86 | ||||
| chr5:132227710-132228170 | Common:4; Rare:110 | ||||
| chr5:132257391-132257791 | Common:15; Rare:150 | ||||
| chr5:132369848-132369956 | Common:3; Rare:39; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:132410760-132411280 | Common:2; Rare:111 | ||||
| chr5:132419730-132419910 | Common:1; Rare:42 |