Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:86968187-86968602 | Common:5; Rare:100 | ||||
chr10:87094036-87094288 | Rare:69 | ||||
chr10:87094327-87094433 | Common:1; Rare:24; Clinvar (benign):2 | ||||
chr10:87094439-87094710 | Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
chr10:87094891-87095238 | Common:1; Rare:83; Clinvar:2 | ||||
chr10:87504785-87504966 | Common:1; Rare:88 | ||||
chr10:87818144-87818366 | Common:2; Rare:78 | ||||
chr10:87863269-87863647 | Common:2; Rare:125; Clinvar:76; Clinvar (benign):8 | ||||
chr10:87864103-87864127 | Rare:6 | ||||
chr10:87864132-87864552 | Common:1; Rare:129; Clinvar:20; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
chr10:88582835-88583007 | Common:2; Rare:54 | ||||
chr10:88583186-88583235 | Rare:27 | ||||
chr10:88583242-88583345 | Rare:25 | ||||
chr10:88583405-88583500 | Rare:17 | ||||
chr10:88880393-88880544 | Common:1; Rare:26 |