Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:174486961-174487385 | Common:2; Rare:100 | ||||
chr2:176002221-176002420 | Common:3; Rare:86 | ||||
chr2:176129586-176129748 | Rare:89 | ||||
chr2:176269389-176269527 | Common:1; Rare:57 | ||||
chr2:177212416-177212802 | Common:4; Rare:158 | ||||
chr2:177263486-177263736 | Common:2; Rare:62 | ||||
chr2:177264651-177264876 | Common:2; Rare:72 | ||||
chr2:177392659-177393005 | Common:3; Rare:122; Clinvar:6; Clinvar (benign):4 | ||||
chr2:178451090-178451418 | Common:6; Rare:99; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478495-178478677 | Common:1; Rare:58 | ||||
chr2:178807212-178807267 | Rare:9 | ||||
chr2:180980246-180980545 | Common:1; Rare:94 | ||||
chr2:180980900-180980959 | Rare:10 | ||||
chr2:182715935-182716323 | Common:3; Rare:136 | ||||
chr2:183124269-183124443 | Common:2; Rare:59 |