Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183223638-183223760 | Common:1; Rare:17 | ||||
chr1:183224279-183224654 | Common:2; Rare:52 | ||||
chr1:183225319-183225516 | Common:1; Rare:30 | ||||
chr1:183232638-183233234 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
chr1:183233348-183233480 | Rare:12 | ||||
chr1:183236413-183236427 | Rare:3 | ||||
chr1:183236444-183236877 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:183241281-183242037 | Common:3; Rare:106 | ||||
chr1:183247338-183247650 | Common:1; Rare:56 | ||||
chr1:183252995-183253102 | Common:1; Rare:17 | ||||
chr1:183257902-183258120 | Rare:26 | ||||
chr1:183258645-183258785 | Common:1; Rare:22 | ||||
chr1:183258842-183258939 | Rare:22 | ||||
chr1:184159362-184159588 | Rare:30 | ||||
chr1:184570463-184570603 | Common:1; Rare:10 |