Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:21674813-21674846 | Rare:7 | ||||
chr13:22884176-22884203 | Common:2; Rare:4 | ||||
chr13:22915740-22915951 | Common:4; Rare:51 | ||||
chr13:24968340-24968668 | Common:13; Rare:60 | ||||
chr13:25468120-25468380 | Rare:43 | ||||
chr13:26012270-26012565 | Common:1; Rare:57 | ||||
chr13:27451226-27451472 | Rare:52 | ||||
chr13:31846527-31846895 | Common:2; Rare:129 | ||||
chr13:40921657-40921749 | Common:1; Rare:30 | ||||
chr13:41192954-41193115 | Rare:33; Clinvar (benign):1 | ||||
chr13:42271378-42271542 | Common:2; Rare:48 | ||||
chr13:43448610-43448831 | Common:1; Rare:30 | ||||
chr13:43785704-43785928 | Rare:63 | ||||
chr13:44142026-44142361 | Common:6; Rare:53 | ||||
chr13:52194370-52194518 | Rare:48 |