Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:128837425-128837667 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr7:128852586-128853030 | Common:4; Rare:132; Clinvar:15; Clinvar (benign):11 | ||||
chr7:131106347-131106546 | Rare:41 | ||||
chr7:131107956-131108210 | Common:1; Rare:41 | ||||
chr7:134826283-134826573 | Common:3; Rare:50 | ||||
chr7:137885736-137886074 | Rare:62 | ||||
chr7:151233267-151233539 | Common:1; Rare:52 | ||||
chr7:152436515-152436859 | Rare:118 | ||||
chr8:2057337-2057780 | Common:5; Rare:194 | ||||
chr8:2115726-2116104 | Common:2; Rare:110 | ||||
chr8:37748015-37748092 | Rare:35 | ||||
chr8:42513187-42513297 | Rare:16 | ||||
chr8:47737307-47737772 | Common:3; Rare:149 | ||||
chr8:56559495-56559541 | Rare:10 | ||||
chr8:66924946-66925103 | Rare:24 |