Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:80078833-80079286 | Common:6; Rare:149 | ||||
chr10:80132573-80132742 | Rare:47 | ||||
chr10:80356735-80356812 | Common:1; Rare:22 | ||||
chr10:80408430-80408615 | Common:1; Rare:58 | ||||
chr10:80453980-80454316 | Common:3; Rare:100 | ||||
chr10:84139301-84139584 | Common:3; Rare:75 | ||||
chr10:84328421-84328685 | Common:2; Rare:93 | ||||
chr10:86957553-86957714 | Rare:39 | ||||
chr10:86968312-86968483 | Common:3; Rare:42 | ||||
chr10:87094995-87095216 | Common:1; Rare:45 | ||||
chr10:87504818-87504948 | Common:1; Rare:68 | ||||
chr10:87817997-87818339 | Common:1; Rare:110 | ||||
chr10:87864211-87864523 | Common:1; Rare:86; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:88582843-88582987 | Common:1; Rare:47 | ||||
chr10:88880166-88880493 | Rare:73 |