Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:227325211-227325445 | Common:5; Rare:76 | ||||
chr2:229921924-229922302 | Common:2; Rare:147 | ||||
chr2:230416155-230416254 | Rare:35 | ||||
chr2:231198529-231198707 | Common:1; Rare:62 | ||||
chr2:232550514-232550720 | Rare:84 | ||||
chr2:232776525-232776738 | Rare:37; Clinvar:1 | ||||
chr2:234495922-234496136 | Rare:64 | ||||
chr2:237085726-237085976 | Common:2; Rare:89 | ||||
chr2:237486365-237486455 | Rare:18 | ||||
chr2:237487136-237487287 | Common:3; Rare:42 | ||||
chr2:237590845-237591134 | Common:6; Rare:53 | ||||
chr2:240025225-240025503 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr2:240560766-240560835 | Rare:29 | ||||
chr2:240561018-240561310 | Common:4; Rare:134 | ||||
chr2:241102280-241102388 | Common:2; Rare:37 |