Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:87345470-87345701 | Common:4; Rare:75 | ||||
chr7:87876224-87876634 | Common:2; Rare:174 | ||||
chr7:88220022-88220149 | Rare:64 | ||||
chr7:90211614-90211905 | Common:4; Rare:89 | ||||
chr7:90245099-90245198 | Rare:33 | ||||
chr7:90346557-90346733 | Common:3; Rare:77 | ||||
chr7:91880667-91880801 | Common:1; Rare:36 | ||||
chr7:91940812-91940989 | Common:4; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92134373-92134603 | Rare:74 | ||||
chr7:92134731-92134888 | Common:3; Rare:45 | ||||
chr7:92245873-92246042 | Common:2; Rare:50; Clinvar:3; Clinvar (benign):4 | ||||
chr7:92246190-92246473 | Common:2; Rare:121 | ||||
chr7:92528370-92528813 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr7:92836560-92836603 | Rare:9 | ||||
chr7:93232139-93232407 | Common:2; Rare:60 |