Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:184051605-184051790 | Common:6; Rare:137 | ||||
chr1:184754768-184755220 | Common:2; Rare:222 | ||||
chr1:185045257-185045595 | Common:2; Rare:114 | ||||
chr1:185156904-185157302 | Common:4; Rare:195 | ||||
chr1:185317175-185317604 | Common:3; Rare:196 | ||||
chr1:186375108-186375554 | Rare:222 | ||||
chr1:186375661-186375977 | Common:2; Rare:156 | ||||
chr1:193059240-193059705 | Rare:421 | ||||
chr1:193105360-193105696 | Common:6; Rare:199 | ||||
chr1:193121678-193122201 | Common:5; Rare:350; Clinvar:10; Clinvar (benign):8 | ||||
chr1:197146587-197146835 | Rare:103; Clinvar:4 | ||||
chr1:197902690-197903160 | Common:4; Rare:330 | ||||
chr1:198156937-198157103 | Rare:63 | ||||
chr1:200042310-200042843 | Common:3; Rare:181 | ||||
chr1:200409954-200410207 | Rare:149 |