Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193059236-193059762 | Common:1; Rare:243 | ||||
chr1:193122032-193122210 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:198156900-198157257 | Common:2; Rare:121 | ||||
chr1:200410016-200410237 | Rare:68 | ||||
chr1:201648565-201648680 | Rare:37 | ||||
chr1:201829084-201829231 | Rare:73 | ||||
chr1:201955209-201955552 | Common:1; Rare:92 | ||||
chr1:202927106-202927362 | Common:5; Rare:111 | ||||
chr1:203626784-203627222 | Common:2; Rare:78 | ||||
chr1:204411776-204412054 | Common:3; Rare:99 | ||||
chr1:205749964-205750073 | Common:3; Rare:44 | ||||
chr1:205813148-205813370 | Common:2; Rare:91 | ||||
chr1:211259475-211259494 | Rare:10 | ||||
chr1:211675597-211675762 | Rare:32 | ||||
chr1:212035501-212035758 | Common:1; Rare:64 |