Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189004030-189004364 | Rare:101; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):20 | ||||
chr2:202376071-202376195 | Rare:56 | ||||
chr2:215408163-215408393 | Common:1; Rare:64 | ||||
chr2:231514362-231514583 | Common:5; Rare:88 | ||||
chr20:18793985-18794086 | Rare:28 | ||||
chr20:19757555-19757606 | Rare:13 | ||||
chr20:36050231-36050308 | Rare:17 | ||||
chr20:36050498-36050646 | Common:1; Rare:58 | ||||
chr20:36050652-36050732 | Rare:30 | ||||
chr20:45824316-45824644 | Common:1; Rare:91 | ||||
chr20:58823472-58823600 | Common:4; Rare:37 | ||||
chr20:62550149-62550453 | Rare:72 | ||||
chr20:62551500-62551625 | Common:1; Rare:32 | ||||
chr21:16194290-16194612 | Common:2; Rare:91 | ||||
chr21:26967069-26967268 | Rare:46 |