Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70411089-70411277 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080939-71081370 | Rare:113 | ||||
chr1:72282669-72282984 | Common:4; Rare:94 | ||||
chr1:74198152-74198331 | Common:2; Rare:106 | ||||
chr1:74733001-74733266 | Common:5; Rare:85 | ||||
chr1:76074617-76074876 | Common:1; Rare:73 | ||||
chr1:77219385-77219498 | Rare:53 | ||||
chr1:77888292-77888745 | Common:2; Rare:101; Clinvar:2 | ||||
chr1:77978988-77979298 | Common:2; Rare:112 | ||||
chr1:78004547-78004951 | Common:4; Rare:94 | ||||
chr1:78490716-78491147 | Common:3; Rare:93; Clinvar:1 | ||||
chr1:83999104-83999454 | Common:6; Rare:104 | ||||
chr1:84077937-84078141 | Common:1; Rare:76 | ||||
chr1:84690462-84690706 | Rare:80 | ||||
chr1:84997064-84997234 | Common:8; Rare:50 |