Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42766546-42766722 | Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:42766984-42767318 | Common:5; Rare:114; Clinvar (benign):1 | ||||
chr1:42817016-42817136 | Common:1; Rare:28 | ||||
chr1:42817203-42817260 | Rare:17 | ||||
chr1:42817263-42817475 | Rare:74 | ||||
chr1:42846401-42846649 | Common:1; Rare:69 | ||||
chr1:42958823-42959013 | Common:2; Rare:47; Clinvar:3; Clinvar (benign):3 | ||||
chr1:43270951-43271002 | Rare:10 | ||||
chr1:43367989-43368159 | Rare:42 | ||||
chr1:43389757-43389950 | Common:3; Rare:86 | ||||
chr1:43946562-43946983 | Rare:113 | ||||
chr1:43974839-43975058 | Common:3; Rare:67 | ||||
chr1:44674411-44674749 | Common:3; Rare:90 | ||||
chr1:44775469-44775600 | Rare:53 | ||||
chr1:44775848-44776140 | Common:2; Rare:108 |