Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:39037969-39038495 | Common:1; Rare:133 | ||||
chr13:39655555-39655724 | Common:3; Rare:94; Clinvar:3; Clinvar (benign):3 | ||||
chr13:40666601-40666805 | Common:2; Rare:68 | ||||
chr13:40771143-40771377 | Common:3; Rare:71 | ||||
chr13:40789374-40789615 | Common:2; Rare:80; Clinvar:5; Clinvar (benign):2 | ||||
chr13:40982861-40983031 | Common:3; Rare:27 | ||||
chr13:41019266-41019457 | Rare:29 | ||||
chr13:41060899-41061068 | Common:16; Rare:95 | ||||
chr13:41061382-41061569 | Common:2; Rare:52 | ||||
chr13:41132735-41132959 | Rare:59 | ||||
chr13:42992223-42992335 | Common:2; Rare:20 | ||||
chr13:42992666-42992924 | Rare:47 | ||||
chr13:43879703-43879843 | Common:17; Rare:49 | ||||
chr13:44989456-44989597 | Rare:49 | ||||
chr13:45340773-45341563 | Common:7; Rare:352 |