Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177552770-177553068 | Common:4; Rare:86 | ||||
chr2:177618706-177618984 | Common:7; Rare:78 | ||||
chr2:178451058-178451372 | Common:6; Rare:94; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178651882-178652183 | Rare:98; Clinvar:12; Clinvar (benign):12 | ||||
chr2:179264508-179264857 | Common:4; Rare:130 | ||||
chr2:180980207-180980545 | Common:2; Rare:101 | ||||
chr2:180980800-180980963 | Rare:41 | ||||
chr2:181891645-181892069 | Common:4; Rare:174 | ||||
chr2:183037994-183038210 | Rare:61 | ||||
chr2:183078680-183078792 | Rare:20 | ||||
chr2:183124252-183124443 | Common:4; Rare:62 | ||||
chr2:186485987-186486360 | Common:3; Rare:108 | ||||
chr2:186589563-186589819 | Rare:50 | ||||
chr2:186590073-186590353 | Rare:83 | ||||
chr2:189441133-189441511 | Common:2; Rare:116 |