Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:227324975-227325378 | Common:8; Rare:130 | ||||
chr2:229922436-229922503 | Rare:19 | ||||
chr2:230416122-230416231 | Rare:35 | ||||
chr2:231464395-231464742 | Common:3; Rare:119 | ||||
chr2:231961390-231961470 | Rare:13 | ||||
chr2:231961648-231961739 | Rare:24; Clinvar:1 | ||||
chr2:232550545-232550719 | Rare:67 | ||||
chr2:232776543-232776699 | Rare:25 | ||||
chr2:233854523-233854724 | Common:4; Rare:45 | ||||
chr2:236569502-236569865 | Common:8; Rare:65 | ||||
chr2:237085769-237085951 | Common:2; Rare:67 | ||||
chr2:238203609-238203937 | Common:3; Rare:130 | ||||
chr2:240025291-240025417 | Common:1; Rare:52; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:241102279-241102425 | Common:2; Rare:46 | ||||
chr2:241272794-241273005 | Rare:74 |