Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:58241311-58241431 | Rare:65; Clinvar:3; Clinvar (benign):1 | ||||
chr2:61017420-61017750 | Common:1; Rare:98; Clinvar:2 | ||||
chr2:61144926-61145164 | Common:3; Rare:79 | ||||
chr2:61538225-61538439 | Common:1; Rare:49 | ||||
chr2:61888584-61888842 | Common:2; Rare:104 | ||||
chr2:63840869-63841149 | Common:2; Rare:76 | ||||
chr2:63841767-63841896 | Common:1; Rare:45 | ||||
chr2:64524089-64524381 | Common:3; Rare:85 | ||||
chr2:64653901-64654073 | Common:1; Rare:60 | ||||
chr2:65227615-65227901 | Rare:84 | ||||
chr2:68062958-68063119 | Common:2; Rare:51 | ||||
chr2:68157515-68157915 | Common:2; Rare:204 | ||||
chr2:68467277-68467599 | Common:1; Rare:78 | ||||
chr2:69387190-69387362 | Rare:43; Clinvar:2 | ||||
chr2:70086954-70087116 | Rare:76 |