Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24793142-24793464 | Rare:140; Clinvar:1 | ||||
chr2:26244578-26244943 | Common:2; Rare:134; Clinvar:6; Clinvar (benign):8 | ||||
chr2:26345828-26346184 | Common:1; Rare:104 | ||||
chr2:27032797-27033016 | Rare:81 | ||||
chr2:27212261-27212366 | Common:1; Rare:54 | ||||
chr2:27356750-27356804 | Rare:10 | ||||
chr2:27370257-27370650 | Common:1; Rare:160 | ||||
chr2:27629006-27629073 | Common:1; Rare:30 | ||||
chr2:27663545-27663911 | Rare:131 | ||||
chr2:28751497-28751868 | Common:4; Rare:167 | ||||
chr2:32039762-32039866 | Rare:31 | ||||
chr2:36355522-36355937 | Common:2; Rare:150 | ||||
chr2:37084293-37084544 | Common:3; Rare:91 | ||||
chr2:37231556-37231689 | Common:4; Rare:70; Clinvar (benign):3 | ||||
chr2:37324724-37324896 | Common:1; Rare:73 |