Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:23453153-23453318 | Rare:53 | ||||
chr18:23503301-23503589 | Common:3; Rare:111 | ||||
chr18:23586393-23586547 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
chr18:24397754-24397984 | Common:2; Rare:91 | ||||
chr18:25352092-25352473 | Common:2; Rare:154 | ||||
chr18:26226302-26226481 | Common:2; Rare:63 | ||||
chr18:31684209-31684355 | Common:2; Rare:40 | ||||
chr18:31943092-31943386 | Common:7; Rare:97 | ||||
chr18:32091826-32091932 | Common:2; Rare:42 | ||||
chr18:32092392-32092732 | Common:5; Rare:151 | ||||
chr18:34976968-34977064 | Common:1; Rare:12 | ||||
chr18:35240909-35241100 | Common:2; Rare:72 | ||||
chr18:35290150-35290372 | Common:2; Rare:72 | ||||
chr18:36067379-36067597 | Rare:83 | ||||
chr18:36129772-36129931 | Common:1; Rare:61 |