Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66332324-66332563 | Rare:67 | ||||
chr1:66533401-66533611 | Common:2; Rare:28 | ||||
chr1:66924760-66925042 | Common:2; Rare:126 | ||||
chr1:66925193-66925518 | Common:2; Rare:101 | ||||
chr1:67053934-67054177 | Common:1; Rare:88 | ||||
chr1:67429989-67430442 | Rare:173 | ||||
chr1:67685795-67686113 | Common:1; Rare:100 | ||||
chr1:67833343-67833527 | Common:2; Rare:72 | ||||
chr1:70205496-70205778 | Rare:101 | ||||
chr1:70354222-70354286 | Common:1; Rare:21 | ||||
chr1:70354654-70354852 | Rare:66 | ||||
chr1:70411029-70411279 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080943-71081383 | Rare:117 | ||||
chr1:72282669-72282974 | Common:4; Rare:89 | ||||
chr1:74198152-74198332 | Common:2; Rare:106 |