Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:127343344-127343429 | Rare:16 | ||||
chr6:127343494-127343515 | Rare:3 | ||||
chr6:127343522-127343645 | Common:1; Rare:36 | ||||
chr6:128520477-128520807 | Common:4; Rare:111 | ||||
chr6:129710088-129710273 | Rare:58 | ||||
chr6:129710305-129710355 | Common:1; Rare:6 | ||||
chr6:131951359-131951623 | Common:2; Rare:53 | ||||
chr6:132814338-132814612 | Common:3; Rare:103 | ||||
chr6:133953052-133953264 | Common:2; Rare:71 | ||||
chr6:134174847-134175029 | Common:1; Rare:86 | ||||
chr6:135054784-135054990 | Common:6; Rare:62 | ||||
chr6:135497604-135497834 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136038314-136038451 | Rare:35 | ||||
chr6:136289756-136290024 | Common:1; Rare:116 | ||||
chr6:138545644-138545842 | Common:1; Rare:39 |