Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:21176524-21176696 | Common:1; Rare:79 | ||||
chr13:23889298-23889468 | Rare:62 | ||||
chr13:24512729-24512839 | Common:3; Rare:33 | ||||
chr13:26221787-26221932 | Rare:36 | ||||
chr13:27450094-27450216 | Common:3; Rare:39 | ||||
chr13:27620574-27620904 | Common:2; Rare:93 | ||||
chr13:30306987-30307211 | Common:5; Rare:57 | ||||
chr13:33285703-33285990 | Common:1; Rare:61 | ||||
chr13:36345535-36345781 | Common:1; Rare:55 | ||||
chr13:36346271-36346534 | Common:3; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
chr13:36999300-36999473 | Rare:66 | ||||
chr13:39037981-39038482 | Common:1; Rare:129 | ||||
chr13:41060854-41061575 | Common:20; Rare:298 | ||||
chr13:41061622-41061661 | Rare:13 | ||||
chr13:41132726-41132949 | Rare:58 |