Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:155854361-155854774 | Rare:115 | ||||
chr3:155870314-155870680 | Common:2; Rare:109 | ||||
chr3:156554982-156555040 | Rare:16 | ||||
chr3:158105677-158105902 | Common:5; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
chr3:158110050-158110197 | Rare:37 | ||||
chr3:158732174-158732241 | Common:2; Rare:20 | ||||
chr3:158801983-158802161 | Common:2; Rare:82 | ||||
chr3:160399169-160399729 | Rare:160; Clinvar:7 | ||||
chr3:160449696-160449885 | Common:1; Rare:68 | ||||
chr3:160565568-160565831 | Common:1; Rare:88 | ||||
chr3:167734810-167735068 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
chr3:167735590-167735735 | Rare:34 | ||||
chr3:168095119-168095213 | Rare:23 | ||||
chr3:169146515-169146666 | Rare:55 | ||||
chr3:169769810-169769965 | Common:4; Rare:33 |