Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:227717981-227718110 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
chr2:227813795-227813849 | Rare:7 | ||||
chr2:229921899-229922511 | Common:4; Rare:213 | ||||
chr2:230416122-230416286 | Rare:51 | ||||
chr2:231464142-231464225 | Rare:23 | ||||
chr2:231464337-231464680 | Common:3; Rare:119 | ||||
chr2:231710314-231710553 | Common:2; Rare:118 | ||||
chr2:231781253-231781478 | Rare:64 | ||||
chr2:231961646-231961755 | Rare:31; Clinvar:1 | ||||
chr2:232550550-232550723 | Rare:66 | ||||
chr2:234951803-234952164 | Common:1; Rare:95 | ||||
chr2:237085742-237085955 | Common:2; Rare:77 | ||||
chr2:237487150-237487298 | Common:2; Rare:38 | ||||
chr2:237966728-237967084 | Common:4; Rare:111 | ||||
chr2:238060760-238061156 | Common:6; Rare:125 |