Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:132638188-132638248 | Rare:23; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr5:133964770-133964942 | Rare:19 | ||||
chr5:134372110-134372411 | Common:1; Rare:59 | ||||
chr5:134374121-134374470 | Rare:57 | ||||
chr5:134383571-134383778 | Common:2; Rare:31 | ||||
chr5:134913689-134914101 | Rare:72 | ||||
chr5:134923439-134923491 | Rare:11 | ||||
chr5:134924047-134924641 | Rare:123 | ||||
chr5:134925420-134925688 | Common:2; Rare:66 | ||||
chr5:134925694-134925854 | Common:1; Rare:30 | ||||
chr5:134927076-134927340 | Common:2; Rare:49 | ||||
chr5:134927668-134927871 | Common:2; Rare:40 | ||||
chr5:134928090-134928329 | Common:3; Rare:45 | ||||
chr5:135993371-135993585 | Common:1; Rare:29 | ||||
chr5:135993893-135993944 | Common:1; Rare:12 |