Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 | ||||
chr7:6447919-6448066 | Common:1; Rare:51 | ||||
chr7:6706927-6707099 | Rare:69 | ||||
chr7:7566789-7567037 | Common:4; Rare:103 | ||||
chr7:12686764-12687043 | Common:3; Rare:91 | ||||
chr7:15686543-15686791 | Common:3; Rare:71 | ||||
chr7:16465736-16465958 | Rare:36 | ||||
chr7:16645686-16646220 | Common:4; Rare:189 | ||||
chr7:17940398-17940574 | Common:1; Rare:89 | ||||
chr7:23105695-23105829 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
chr7:23181864-23182083 | Common:1; Rare:90 | ||||
chr7:23299193-23299437 | Common:2; Rare:128 | ||||
chr7:23470358-23470517 | Rare:50 | ||||
chr7:25125245-25125643 | Rare:156; Clinvar:3 | ||||
chr7:26200657-26201271 | Common:3; Rare:289 |