Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:519105-519265 | Rare:41 | ||||
chr7:727217-727297 | Rare:29; Clinvar:2 | ||||
chr7:1055129-1055393 | Common:1; Rare:94 | ||||
chr7:1570015-1570142 | Common:1; Rare:41 | ||||
chr7:2242162-2242262 | Common:2; Rare:61 | ||||
chr7:2354054-2354117 | Rare:31 | ||||
chr7:4775510-4775697 | Common:4; Rare:88; Clinvar:1 | ||||
chr7:6009023-6009469 | Common:4; Rare:205; Clinvar:8; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
chr7:6374638-6374769 | Common:1; Rare:30 | ||||
chr7:6399874-6400183 | Rare:69 | ||||
chr7:6401695-6402027 | Rare:64 | ||||
chr7:6447940-6448055 | Common:1; Rare:39 | ||||
chr7:7566748-7567073 | Common:5; Rare:127 | ||||
chr7:7567160-7567418 | Common:1; Rare:88 | ||||
chr7:12211190-12211420 | Common:3; Rare:95 |