Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:132886359-132886480 | Rare:30 | ||||
chr5:134465845-134465972 | Rare:38 | ||||
chr5:134506146-134506514 | Common:1; Rare:75 | ||||
chr5:134927128-134927187 | Rare:15 | ||||
chr5:134927730-134927746 | Rare:3 | ||||
chr5:135352993-135353148 | Rare:39 | ||||
chr5:135354944-135355140 | Common:1; Rare:35 | ||||
chr5:135357153-135357392 | Common:2; Rare:41 | ||||
chr5:136191821-136191902 | Common:1; Rare:20 | ||||
chr5:136193130-136193221 | Common:2; Rare:23 | ||||
chr5:138951250-138951485 | Common:2; Rare:61; Clinvar (benign):3 | ||||
chr5:139391727-139391851 | Rare:22 | ||||
chr5:140228444-140228566 | Rare:18 | ||||
chr5:140250521-140250645 | Rare:13 | ||||
chr5:140401115-140401241 | Common:1; Rare:25 |