Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1013367-1013549 | Common:4; Rare:57 | ||||
chr1:1045804-1046088 | Rare:135; Clinvar:6; Clinvar (benign):6 | ||||
chr1:1047684-1047806 | Rare:50 | ||||
chr1:1308372-1308652 | Common:8; Rare:123 | ||||
chr1:1324586-1324932 | Common:3; Rare:164 | ||||
chr1:1375169-1375557 | Common:6; Rare:103 | ||||
chr1:1399229-1399575 | Common:1; Rare:161 | ||||
chr1:1574553-1574978 | Common:1; Rare:199 | ||||
chr1:1658932-1659218 | Common:4; Rare:114 | ||||
chr1:1724279-1724467 | Common:3; Rare:67 | ||||
chr1:2391514-2391948 | Common:2; Rare:152 | ||||
chr1:3796492-3796635 | Common:2; Rare:45 | ||||
chr1:3857209-3857513 | Common:1; Rare:77 | ||||
chr1:3900182-3900427 | Common:12; Rare:116 | ||||
chr1:5992389-5992704 | Common:4; Rare:107; Clinvar:6 |