Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70410968-70411431 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
chr1:70411448-70411774 | Rare:84 | ||||
chr1:71047726-71047977 | Common:3; Rare:50 | ||||
chr1:71080311-71080584 | Common:1; Rare:66 | ||||
chr1:71080803-71081417 | Rare:179 | ||||
chr1:72282501-72282987 | Common:7; Rare:137 | ||||
chr1:74198051-74198443 | Common:3; Rare:177 | ||||
chr1:74732538-74732791 | Common:4; Rare:55 | ||||
chr1:74733008-74733337 | Common:6; Rare:119 | ||||
chr1:74733393-74733489 | Rare:41 | ||||
chr1:74733817-74734028 | Common:2; Rare:43 | ||||
chr1:75724271-75724441 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr1:75724526-75724772 | Common:3; Rare:104; Clinvar:5; Clinvar (benign):3 | ||||
chr1:75785724-75786314 | Common:4; Rare:184 | ||||
chr1:75786449-75786804 | Common:6; Rare:82 |