Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70086944-70087118 | Rare:83 | ||||
chr2:70190955-70191150 | Common:1; Rare:51 | ||||
chr2:70225078-70225460 | Common:1; Rare:71 | ||||
chr2:70257925-70258258 | Common:2; Rare:110 | ||||
chr2:70293676-70293821 | Common:2; Rare:47 | ||||
chr2:70301950-70302249 | Common:5; Rare:128 | ||||
chr2:70767900-70767956 | Rare:17 | ||||
chr2:70768087-70768271 | Common:2; Rare:37 | ||||
chr2:70994730-70994893 | Common:3; Rare:60 | ||||
chr2:71068523-71068697 | Rare:81 | ||||
chr2:71129716-71129964 | Rare:50 | ||||
chr2:71130220-71130807 | Common:7; Rare:186; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71276383-71276660 | Rare:108 | ||||
chr2:73071256-73071511 | Common:1; Rare:94 | ||||
chr2:73071692-73071861 | Common:2; Rare:66 |