Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24502699-24502998 | Common:1; Rare:69 | ||||
chr13:28228426-28228710 | Common:1; Rare:45 | ||||
chr13:29524131-29524454 | Common:1; Rare:81 | ||||
chr13:29677062-29677163 | Common:1; Rare:17 | ||||
chr13:33676783-33676899 | Common:2; Rare:28 | ||||
chr13:37007917-37008175 | Rare:65 | ||||
chr13:41060121-41060382 | Common:3; Rare:86 | ||||
chr13:44142015-44142337 | Common:6; Rare:48 | ||||
chr13:48379918-48380080 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr13:48412990-48413219 | Rare:32 | ||||
chr13:48504334-48504638 | Common:4; Rare:52 | ||||
chr13:48580892-48581237 | Common:1; Rare:61 | ||||
chr13:52194392-52194510 | Rare:36 | ||||
chr13:52617321-52617547 | Common:1; Rare:56 | ||||
chr13:73059315-73059586 | Rare:63 |