Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:43106018-43106198 | Rare:58 | ||||
chr15:43330594-43330716 | Rare:42 | ||||
chr15:43370908-43371108 | Common:3; Rare:54 | ||||
chr15:43493069-43493340 | Common:1; Rare:88 | ||||
chr15:43510700-43510954 | Rare:78 | ||||
chr15:43746287-43746446 | Common:1; Rare:61 | ||||
chr15:43746566-43746690 | Rare:47 | ||||
chr15:43776949-43777091 | Common:1; Rare:41 | ||||
chr15:43777114-43777127 | Rare:5 | ||||
chr15:43792676-43793030 | Rare:102 | ||||
chr15:43824623-43824738 | Rare:28 | ||||
chr15:44536666-44537412 | Common:3; Rare:244 | ||||
chr15:44711265-44711612 | Rare:98; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr15:44711804-44711959 | Rare:32 | ||||
chr15:44728869-44729196 | Common:1; Rare:70 |