Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:68467267-68467616 | Common:1; Rare:91 | ||||
chr2:69387178-69387398 | Rare:59; Clinvar:2 | ||||
chr2:69829373-69829729 | Rare:132 | ||||
chr2:70087433-70087777 | Rare:133 | ||||
chr2:70257902-70258167 | Common:1; Rare:83 | ||||
chr2:70293667-70293852 | Common:3; Rare:59 | ||||
chr2:71068526-71068654 | Rare:64 | ||||
chr2:71130225-71130682 | Common:6; Rare:132; Clinvar:1; Clinvar (benign):2 | ||||
chr2:73071707-73071888 | Common:2; Rare:67 | ||||
chr2:73234219-73234356 | Common:1; Rare:40 | ||||
chr2:73385694-73386023 | Common:4; Rare:155; Clinvar:16; Clinvar (benign):8 | ||||
chr2:74147845-74148111 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74178800-74179002 | Common:2; Rare:54 | ||||
chr2:74421628-74421759 | Rare:42 | ||||
chr2:74482924-74483113 | Common:1; Rare:68 |