Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67430083-67430591 | Rare:185 | ||||
chr1:67833342-67833512 | Common:2; Rare:69 | ||||
chr1:68496501-68496712 | Common:2; Rare:44 | ||||
chr1:68497023-68497196 | Common:2; Rare:61 | ||||
chr1:70205515-70205787 | Rare:95 | ||||
chr1:70221296-70221519 | Rare:97 | ||||
chr1:70231917-70232120 | Rare:31 | ||||
chr1:70354674-70354872 | Rare:65 | ||||
chr1:70411089-70411290 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080945-71081393 | Rare:123 | ||||
chr1:72282923-72282975 | Common:1; Rare:27 | ||||
chr1:74198068-74198360 | Common:3; Rare:147 | ||||
chr1:74578664-74578791 | Common:1; Rare:22 | ||||
chr1:74579461-74579508 | Rare:11 | ||||
chr1:74732994-74733456 | Common:6; Rare:166 |