Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:84077937-84078124 | Common:1; Rare:67 | ||||
chr1:88684025-88684292 | Common:3; Rare:78 | ||||
chr1:92298977-92299067 | Common:1; Rare:43; Clinvar:1 | ||||
chr1:93180344-93180668 | Common:1; Rare:130 | ||||
chr1:94927023-94927464 | Common:3; Rare:146 | ||||
chr1:100266114-100266265 | Common:2; Rare:58 | ||||
chr1:100894840-100894914 | Rare:15 | ||||
chr1:101025763-101025910 | Common:1; Rare:44 | ||||
chr1:109548507-109548645 | Common:1; Rare:49 | ||||
chr1:111140069-111140263 | Common:1; Rare:68 | ||||
chr1:112396009-112396265 | Common:1; Rare:80 | ||||
chr1:112619112-112619236 | Rare:43 | ||||
chr1:112619798-112619838 | Common:1; Rare:19 | ||||
chr1:145927419-145927648 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964593-145964754 | Rare:35 |