Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:231708263-231708746 | Common:4; Rare:213 | ||||
chr2:231708878-231708951 | Rare:32 | ||||
chr2:231710306-231710527 | Common:2; Rare:109 | ||||
chr2:231781247-231781446 | Rare:57 | ||||
chr2:231961648-231961748 | Rare:29; Clinvar:1 | ||||
chr2:232550545-232550727 | Rare:73 | ||||
chr2:233251486-233251710 | Common:3; Rare:77 | ||||
chr2:233854505-233854755 | Common:4; Rare:68 | ||||
chr2:237085748-237085946 | Common:2; Rare:68 | ||||
chr2:237487029-237487288 | Common:4; Rare:59 | ||||
chr2:237966728-237967074 | Common:3; Rare:107 | ||||
chr2:238060841-238061022 | Common:3; Rare:58 | ||||
chr2:238203598-238203797 | Common:3; Rare:83 | ||||
chr2:240025291-240025480 | Common:1; Rare:75; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:240136262-240136403 | Common:1; Rare:63 |