Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24971953-24972148 | Common:1; Rare:53 | ||||
chr2:26033769-26034146 | Common:4; Rare:139 | ||||
chr2:26244594-26244956 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):7 | ||||
chr2:26345789-26346152 | Common:1; Rare:105 | ||||
chr2:27078531-27078955 | Common:3; Rare:103 | ||||
chr2:27211921-27212088 | Common:3; Rare:63 | ||||
chr2:27212236-27212379 | Common:1; Rare:75 | ||||
chr2:27217145-27217378 | Rare:67 | ||||
chr2:27356751-27357081 | Rare:93 | ||||
chr2:27370257-27370685 | Common:2; Rare:176 | ||||
chr2:27628981-27629073 | Common:1; Rare:45 | ||||
chr2:27663402-27663934 | Rare:172 | ||||
chr2:27890348-27890786 | Common:1; Rare:120 | ||||
chr2:28751719-28751868 | Common:2; Rare:82 | ||||
chr2:31233974-31234247 | Rare:70 |