Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:231707532-231707581 | Rare:15 | ||||
chr2:231707778-231707835 | Common:1; Rare:20 | ||||
chr2:231708348-231708746 | Common:3; Rare:181 | ||||
chr2:231708832-231708990 | Common:2; Rare:71 | ||||
chr2:231710278-231710527 | Common:2; Rare:124 | ||||
chr2:231781241-231781415 | Rare:47 | ||||
chr2:231961648-231961748 | Rare:29; Clinvar:1 | ||||
chr2:232550545-232550581 | Rare:12 | ||||
chr2:232550584-232550716 | Rare:50 | ||||
chr2:232632936-232633280 | Common:4; Rare:78 | ||||
chr2:234951803-234952133 | Common:1; Rare:86 | ||||
chr2:237085719-237085955 | Common:2; Rare:81 | ||||
chr2:237414017-237414400 | Common:2; Rare:76; Clinvar (benign):3 | ||||
chr2:237487132-237487283 | Common:3; Rare:40 | ||||
chr2:237591093-237591206 | Common:1; Rare:35 |