Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7352088-7352207 | Rare:35 | ||||
chr17:7438055-7438339 | Common:1; Rare:60 | ||||
chr17:7455511-7455861 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7479508-7479740 | Common:1; Rare:41 | ||||
chr17:7484239-7484370 | Common:1; Rare:53 | ||||
chr17:7499159-7499323 | Common:2; Rare:48 | ||||
chr17:7549006-7549237 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr17:7558167-7558324 | Rare:33 | ||||
chr17:7558828-7559022 | Common:1; Rare:44 | ||||
chr17:7583542-7583864 | Common:1; Rare:131; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7592855-7593123 | Common:1; Rare:80 | ||||
chr17:7614501-7614682 | Rare:47 | ||||
chr17:7627712-7627983 | Common:3; Rare:92 | ||||
chr17:7857100-7857633 | Common:3; Rare:225 | ||||
chr17:7857805-7858066 | Common:2; Rare:87 |