Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89022721-89022897 | Rare:31 | ||||
chr1:89065174-89065458 | Common:2; Rare:46 | ||||
chr1:89126024-89126159 | Rare:33 | ||||
chr1:89198838-89199001 | Common:1; Rare:29 | ||||
chr1:89632966-89633227 | Common:3; Rare:75 | ||||
chr1:89821029-89821223 | Common:1; Rare:62 | ||||
chr1:89821611-89821696 | Rare:25 | ||||
chr1:89821782-89822013 | Rare:63 | ||||
chr1:89994973-89995221 | Common:2; Rare:91 | ||||
chr1:91021943-91022451 | Common:1; Rare:121 | ||||
chr1:91500568-91500901 | Common:3; Rare:82 | ||||
chr1:91886006-91886366 | Rare:141 | ||||
chr1:92029930-92030052 | Rare:33 | ||||
chr1:92080420-92080584 | Common:1; Rare:51 | ||||
chr1:92298889-92299094 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):2 |