Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:149749555-149749796 | Rare:113 | ||||
chr6:149963824-149964031 | Common:1; Rare:69 | ||||
chr6:151240218-151240227 | Common:1; Rare:1 | ||||
chr6:151240234-151240427 | Common:1; Rare:51 | ||||
chr6:151391490-151391764 | Common:3; Rare:72 | ||||
chr6:151452029-151452552 | Common:4; Rare:184 | ||||
chr6:152982975-152983287 | Common:2; Rare:97 | ||||
chr6:152983487-152983709 | Common:2; Rare:76 | ||||
chr6:153002643-153002838 | Common:3; Rare:70 | ||||
chr6:155314456-155314613 | Common:2; Rare:48 | ||||
chr6:157323497-157323597 | Common:2; Rare:37 | ||||
chr6:158168142-158168388 | Common:3; Rare:90; Clinvar (benign):2 | ||||
chr6:158644686-158644930 | Common:3; Rare:100 | ||||
chr6:158818161-158818407 | Common:4; Rare:95 | ||||
chr6:158819316-158819446 | Common:2; Rare:49 |