Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:35185198-35185374 | Rare:37 | ||||
chr1:35186942-35187152 | Rare:68 | ||||
chr1:35189002-35189384 | Common:3; Rare:104 | ||||
chr1:35387202-35387476 | Rare:56 | ||||
chr1:35438277-35438334 | Common:2; Rare:4 | ||||
chr1:37802568-37802801 | Common:1; Rare:48 | ||||
chr1:39158700-39158894 | Common:1; Rare:47 | ||||
chr1:41012509-41012684 | Common:2; Rare:27 | ||||
chr1:41031317-41031336 | Rare:5 | ||||
chr1:41168091-41168262 | Common:1; Rare:33 | ||||
chr1:42666457-42666585 | Rare:32 | ||||
chr1:42929588-42929910 | Common:1; Rare:85; Clinvar:8; Clinvar (benign):13; Clinvar (pathogenic):6 | ||||
chr1:43166815-43167257 | Common:5; Rare:101 | ||||
chr1:44807342-44807608 | Common:1; Rare:54 | ||||
chr1:45514600-45514981 | Rare:100 |