Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:122974566-122974817 | Rare:56 | ||||
chr12:122975133-122975248 | Common:1; Rare:31 | ||||
chr12:122980570-122980941 | Common:2; Rare:108 | ||||
chr12:123232774-123232917 | Common:4; Rare:36 | ||||
chr12:123233087-123233494 | Common:2; Rare:137; Clinvar:1 | ||||
chr12:123364725-123364977 | Common:5; Rare:116 | ||||
chr12:123383820-123384206 | Rare:87 | ||||
chr12:123436437-123436672 | Rare:53 | ||||
chr12:123584307-123584813 | Common:9; Rare:170 | ||||
chr12:123602010-123602190 | Common:3; Rare:62 | ||||
chr12:123633544-123633902 | Common:2; Rare:168; Clinvar:8; Clinvar (benign):1 | ||||
chr12:124388794-124388978 | Common:3; Rare:54 | ||||
chr12:124863647-124864042 | Common:5; Rare:108 | ||||
chr12:124914575-124915057 | Common:9; Rare:199 | ||||
chr12:124917750-124917792 | Rare:14 |