Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45340114-45340178 | Rare:23 | ||||
chr1:45500044-45500358 | Common:1; Rare:76; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521865-45522033 | Common:1; Rare:66 | ||||
chr1:45583931-45584060 | Rare:47 | ||||
chr1:45687059-45687229 | Common:1; Rare:55 | ||||
chr1:45688055-45688211 | Common:1; Rare:39 | ||||
chr1:46198389-46198518 | Common:1; Rare:51; Clinvar:1 | ||||
chr1:46303308-46303769 | Common:2; Rare:127 | ||||
chr1:46340658-46340801 | Common:2; Rare:35 | ||||
chr1:47314101-47314434 | Common:3; Rare:69; Clinvar:1 | ||||
chr1:50970097-50970274 | Rare:33 | ||||
chr1:52056174-52056343 | Rare:50 | ||||
chr1:52404467-52404629 | Common:1; Rare:49 | ||||
chr1:52552974-52553386 | Common:4; Rare:125 | ||||
chr1:53220581-53220690 | Common:1; Rare:50 |