Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74370464-74370820 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
chr2:75673379-75673545 | Rare:51 | ||||
chr2:88016540-88017103 | Common:13; Rare:195 | ||||
chr2:91659908-91660053 | Rare:25 | ||||
chr2:94622457-94622653 | Common:1; Rare:54 | ||||
chr2:94667380-94667570 | Rare:48 | ||||
chr2:95526693-95526909 | Common:1; Rare:71 | ||||
chr2:96010501-96010611 | Rare:23 | ||||
chr2:104406405-104406560 | Common:1; Rare:37 | ||||
chr2:104434124-104434501 | Common:1; Rare:71 | ||||
chr2:104756156-104756375 | Rare:46 | ||||
chr2:104843436-104843760 | Common:1; Rare:65 | ||||
chr2:104851417-104851714 | Rare:48 | ||||
chr2:104853151-104853378 | Common:2; Rare:48 | ||||
chr2:104853715-104854327 | Common:3; Rare:181 |