Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155308632-155309019 | Common:1; Rare:84 | ||||
chr1:155324195-155324562 | Common:2; Rare:136 | ||||
chr1:155859361-155859578 | Common:2; Rare:52 | ||||
chr1:156054611-156054871 | Common:3; Rare:72 | ||||
chr1:156135987-156136299 | Common:3; Rare:101; Clinvar:15; Clinvar (benign):14; Clinvar (pathogenic):8 | ||||
chr1:156212727-156213031 | Common:1; Rare:65 | ||||
chr1:156282797-156282947 | Common:2; Rare:41 | ||||
chr1:156728388-156728475 | Common:1; Rare:15 | ||||
chr1:156767379-156767607 | Common:1; Rare:70 | ||||
chr1:157138337-157138453 | Common:2; Rare:29 | ||||
chr1:160343178-160343418 | Rare:98 | ||||
chr1:161045879-161046060 | Common:1; Rare:47 | ||||
chr1:161117953-161118146 | Rare:96 | ||||
chr1:161132409-161132679 | Common:1; Rare:91 | ||||
chr1:161197200-161197428 | Common:2; Rare:40 |