Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:44251730-44252267 | Common:3; Rare:181 | ||||
chr6:57961358-57961638 | Common:2; Rare:86 | ||||
chr6:71420119-71420361 | Common:1; Rare:78 | ||||
chr6:73517858-73518265 | Common:2; Rare:108 | ||||
chr6:85678668-85678984 | Rare:126 | ||||
chr6:118537549-118537843 | Rare:52 | ||||
chr6:123439214-123439752 | Common:5; Rare:87 | ||||
chr6:129391215-129391651 | Common:1; Rare:108; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr6:132131829-132132055 | Rare:41 | ||||
chr6:132817023-132817087 | Rare:23 | ||||
chr6:137218493-137218652 | Common:3; Rare:28 | ||||
chr6:137218764-137218843 | Rare:10 | ||||
chr6:138864711-138864877 | Common:2; Rare:31 | ||||
chr6:141403276-141403437 | Common:1; Rare:38 | ||||
chr6:142885534-142885660 | Rare:16 |