Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21860178-21860414 | Rare:58; Clinvar:1 | ||||
chr1:21872304-21872528 | Common:1; Rare:60; Clinvar:2 | ||||
chr1:21875865-21876313 | Common:1; Rare:139; Clinvar:6; Clinvar (benign):1 | ||||
chr1:21884818-21885149 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
chr1:21887215-21887694 | Common:3; Rare:182; Clinvar:13; Clinvar (benign):3 | ||||
chr1:21890097-21890497 | Common:1; Rare:106; Clinvar (benign):1 | ||||
chr1:22509955-22510161 | Common:1; Rare:33 | ||||
chr1:24798984-24799148 | Common:2; Rare:47 | ||||
chr1:26942690-26942943 | Rare:93 | ||||
chr1:27598244-27598554 | Common:2; Rare:58 | ||||
chr1:27602494-27602530 | Rare:6 | ||||
chr1:28581726-28581773 | Rare:15 | ||||
chr1:29181067-29181349 | Common:1; Rare:65 | ||||
chr1:31695152-31695222 | Rare:27 | ||||
chr1:31701584-31701661 | Rare:14 |