Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:23557318-23557557 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
chr16:23641212-23641560 | Common:2; Rare:101; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24729604-24729789 | Common:7; Rare:84 | ||||
chr16:25015324-25015461 | Common:2; Rare:48 | ||||
chr16:25111453-25111792 | Common:2; Rare:87 | ||||
chr16:27268724-27268916 | Common:1; Rare:69 | ||||
chr16:27549861-27550167 | Common:2; Rare:119 | ||||
chr16:28538871-28539187 | Common:2; Rare:69 | ||||
chr16:28846253-28846643 | Common:2; Rare:133; Clinvar:6; Clinvar (benign):6 | ||||
chr16:28863735-28863979 | Common:3; Rare:58 | ||||
chr16:28925159-28925354 | Rare:57 | ||||
chr16:28974676-28974792 | Rare:53 | ||||
chr16:29961879-29962137 | Common:1; Rare:75 | ||||
chr16:29995610-29995719 | Rare:50 | ||||
chr16:29996064-29996289 | Common:2; Rare:81 |