Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122163212-122163642 | Common:4; Rare:106 | ||||
chr10:122953793-122953909 | Common:1; Rare:19 | ||||
chr10:122954166-122954492 | Rare:118 | ||||
chr10:122980354-122980492 | Common:1; Rare:41 | ||||
chr10:122980633-122980772 | Common:2; Rare:55 | ||||
chr10:123008693-123009044 | Common:6; Rare:95; Clinvar:4; Clinvar (benign):5 | ||||
chr10:123891755-123892115 | Common:1; Rare:102 | ||||
chr10:124092713-124092998 | Common:1; Rare:60 | ||||
chr10:124093477-124093681 | Common:2; Rare:37 | ||||
chr10:124418878-124419099 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
chr10:124461650-124461907 | Common:5; Rare:82 | ||||
chr10:124791445-124791591 | Rare:28 | ||||
chr10:124791721-124791944 | Common:1; Rare:116 | ||||
chr10:124801749-124801861 | Rare:43 | ||||
chr10:125158706-125158860 | Rare:45 |