Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:633747-634021 | Common:6; Rare:99 | ||||
chr1:778598-778820 | Common:4; Rare:95 | ||||
chr1:827427-827836 | Common:3; Rare:131 | ||||
chr1:946218-946540 | Common:3; Rare:146 | ||||
chr1:1069935-1070228 | Common:1; Rare:57 | ||||
chr1:1348102-1348131 | Rare:12 | ||||
chr1:2428582-2428723 | Common:1; Rare:37 | ||||
chr1:3707307-3707595 | Common:1; Rare:85 | ||||
chr1:9182106-9182235 | Rare:34 | ||||
chr1:9242714-9242848 | Common:1; Rare:34 | ||||
chr1:9244757-9244971 | Common:2; Rare:55; Clinvar (benign):1 | ||||
chr1:9687517-9687640 | Common:1; Rare:33 | ||||
chr1:11087885-11088157 | Common:3; Rare:75 | ||||
chr1:11965338-11965575 | Common:3; Rare:81; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:12619004-12619220 | Rare:39 |