Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50373168-50373235 | Common:2; Rare:28 | ||||
chr17:50719467-50719647 | Rare:70 | ||||
chr17:50866354-50866547 | Common:2; Rare:61 | ||||
chr17:51260312-51260669 | Common:4; Rare:166 | ||||
chr17:54968601-54968792 | Common:3; Rare:90 | ||||
chr17:56914016-56914177 | Rare:42 | ||||
chr17:57084999-57085096 | Rare:37 | ||||
chr17:57850006-57850274 | Common:1; Rare:86 | ||||
chr17:58219216-58219424 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):4 | ||||
chr17:59106707-59106941 | Common:2; Rare:72; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59331425-59331778 | Common:3; Rare:114 | ||||
chr17:59619557-59620091 | Common:3; Rare:185 | ||||
chr17:59707390-59707732 | Common:3; Rare:95; Clinvar (benign):4 | ||||
chr17:59837609-59837993 | Rare:55 | ||||
chr17:59892714-59893139 | Rare:112 |