Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:74730123-74730159 | Common:1; Rare:17 | ||||
chr1:75794085-75794577 | Common:3; Rare:106 | ||||
chr1:77569894-77569988 | Common:2; Rare:20 | ||||
chr1:77773028-77773142 | Rare:17 | ||||
chr1:77774529-77774609 | Rare:27 | ||||
chr1:77791274-77791298 | Rare:3 | ||||
chr1:77848045-77848116 | Rare:17 | ||||
chr1:77915795-77916069 | Rare:47; Clinvar (benign):3 | ||||
chr1:77964946-77965229 | Common:3; Rare:85 | ||||
chr1:77994493-77994569 | Rare:14 | ||||
chr1:78648644-78648691 | Rare:11 | ||||
chr1:78656200-78656460 | Rare:48 | ||||
chr1:78661715-78661878 | Rare:36 | ||||
chr1:81723487-81723763 | Common:1; Rare:45 | ||||
chr1:84526944-84527197 | Common:2; Rare:43 |