Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:149749523-149749800 | Rare:123 | ||||
chr6:150866223-150866539 | Rare:123 | ||||
chr6:151240234-151240437 | Common:1; Rare:54 | ||||
chr6:151325409-151325720 | Common:2; Rare:72 | ||||
chr6:151391503-151391779 | Common:3; Rare:70 | ||||
chr6:151452029-151452548 | Common:4; Rare:183 | ||||
chr6:152381307-152381433 | Rare:37; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr6:152983017-152983391 | Common:2; Rare:116 | ||||
chr6:152983499-152983715 | Common:3; Rare:78 | ||||
chr6:155314447-155314764 | Common:10; Rare:115 | ||||
chr6:157323495-157323658 | Common:3; Rare:50 | ||||
chr6:158168225-158168388 | Common:2; Rare:59 | ||||
chr6:158644686-158645003 | Common:3; Rare:113 | ||||
chr6:158649925-158650067 | Rare:34 | ||||
chr6:158818209-158818355 | Common:4; Rare:56 |