Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42924279-42924461 | Common:1; Rare:55 | ||||
chr1:43106755-43106920 | Common:1; Rare:34 | ||||
chr1:43348858-43349221 | Common:2; Rare:120; Clinvar:5; Clinvar (benign):1 | ||||
chr1:43417764-43418012 | Rare:47 | ||||
chr1:43666886-43667005 | Rare:21 | ||||
chr1:43667646-43667813 | Rare:27 | ||||
chr1:43873129-43873257 | Common:1; Rare:31 | ||||
chr1:43877269-43877375 | Rare:20 | ||||
chr1:44035869-44036078 | Rare:38 | ||||
chr1:44043766-44043954 | Common:1; Rare:40 | ||||
chr1:44223143-44223432 | Common:2; Rare:66 | ||||
chr1:44645109-44645276 | Common:2; Rare:51 | ||||
chr1:45205844-45205999 | Common:1; Rare:55 | ||||
chr1:45303590-45303893 | Common:1; Rare:83 | ||||
chr1:45616397-45616692 | Common:2; Rare:81 |