Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:33274873-33275048 | Rare:37 | ||||
chr13:33275594-33275633 | Common:1; Rare:7 | ||||
chr13:33277110-33277185 | Rare:12 | ||||
chr13:33282034-33282080 | Rare:5 | ||||
chr13:36305112-36305336 | Rare:34 | ||||
chr13:36337311-36337455 | Common:1; Rare:27 | ||||
chr13:36964794-36964967 | Common:4; Rare:30 | ||||
chr13:37596667-37596932 | Rare:47 | ||||
chr13:38355907-38356169 | Common:3; Rare:41 | ||||
chr13:41062454-41062661 | Common:2; Rare:55 | ||||
chr13:41078885-41079130 | Common:3; Rare:72 | ||||
chr13:41079325-41079332 | Rare:2 | ||||
chr13:41192619-41192642 | Rare:5 | ||||
chr13:41192932-41193073 | Rare:33; Clinvar (benign):1 | ||||
chr13:41366755-41366980 | Common:1; Rare:34 |