Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67685952-67686080 | Common:1; Rare:53 | ||||
chr1:68232201-68232307 | Rare:26 | ||||
chr1:68496963-68497233 | Common:2; Rare:96 | ||||
chr1:70205542-70205807 | Rare:79 | ||||
chr1:70221338-70221837 | Rare:185 | ||||
chr1:70227688-70227965 | Common:2; Rare:56 | ||||
chr1:70230945-70231061 | Rare:13 | ||||
chr1:70246848-70247076 | Rare:46 | ||||
chr1:70354677-70354862 | Rare:65 | ||||
chr1:71080945-71081397 | Rare:124 | ||||
chr1:72283212-72283408 | Rare:45 | ||||
chr1:74198123-74198338 | Common:3; Rare:118 | ||||
chr1:74732973-74733276 | Common:5; Rare:95 | ||||
chr1:75724626-75724815 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):2 | ||||
chr1:75786804-75786868 | Rare:7 |