Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153976971-153977321 | Common:1; Rare:95 | ||||
chr1:153986259-153986581 | Common:1; Rare:72 | ||||
chr1:153990668-153990846 | Common:2; Rare:93 | ||||
chr1:154172884-154173173 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:154182621-154182813 | Common:1; Rare:45 | ||||
chr1:154182896-154182964 | Rare:21 | ||||
chr1:154182981-154183029 | Rare:12 | ||||
chr1:154183141-154183457 | Rare:95 | ||||
chr1:154219786-154220262 | Common:5; Rare:138 | ||||
chr1:154220306-154221224 | Common:1; Rare:297 | ||||
chr1:154221245-154221407 | Rare:36 | ||||
chr1:154221436-154221716 | Rare:75 | ||||
chr1:154254742-154254864 | Common:2; Rare:28 | ||||
chr1:154257063-154257434 | Rare:94 | ||||
chr1:154261935-154262059 | Rare:25 |