Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25906392-25906586 | Rare:75 | ||||
chr1:26432123-26432390 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472276-26472528 | Common:4; Rare:81 | ||||
chr1:26787865-26787978 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr1:26890205-26890344 | Common:1; Rare:51 | ||||
chr1:28328894-28329062 | Common:1; Rare:55 | ||||
chr1:28505815-28506062 | Common:2; Rare:99 | ||||
chr1:28552847-28553113 | Common:2; Rare:99 | ||||
chr1:28643020-28643164 | Rare:61 | ||||
chr1:28736698-28737018 | Common:2; Rare:105 | ||||
chr1:28737716-28737769 | Rare:19 | ||||
chr1:31065651-31065957 | Common:2; Rare:110 | ||||
chr1:31296743-31297076 | Common:5; Rare:109 | ||||
chr1:32072845-32072993 | Rare:42 | ||||
chr1:32222329-32222582 | Rare:96 |