Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:108562704-108562879 | Common:1; Rare:51 | ||||
chr6:108654085-108654392 | Common:4; Rare:50 | ||||
chr6:111559643-111559890 | Common:1; Rare:46 | ||||
chr6:112119278-112119411 | Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
chr6:116253353-116253604 | Rare:74 | ||||
chr6:117578947-117579270 | Rare:63 | ||||
chr6:118558622-118558931 | Common:15; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
chr6:118895098-118895253 | Rare:43 | ||||
chr6:119350594-119350737 | Common:2; Rare:30 | ||||
chr6:127120771-127120836 | Rare:17 | ||||
chr6:129459937-129460311 | Common:2; Rare:92; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr6:131950078-131950543 | Common:1; Rare:146 | ||||
chr6:132817023-132817326 | Common:3; Rare:109 | ||||
chr6:135498415-135498469 | Rare:14 | ||||
chr6:137868174-137868249 | Rare:12 |