Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5419639-5419869 | Common:3; Rare:70 | ||||
chr17:5420110-5420239 | Rare:55 | ||||
chr17:5486157-5486602 | Common:5; Rare:152 | ||||
chr17:5486796-5486921 | Common:4; Rare:38 | ||||
chr17:6556398-6556722 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
chr17:6640645-6641084 | Common:7; Rare:135 | ||||
chr17:6651542-6651752 | Common:1; Rare:72 | ||||
chr17:6755852-6756085 | Common:4; Rare:53 | ||||
chr17:7012306-7012692 | Rare:133 | ||||
chr17:7219728-7219949 | Common:3; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr17:7224366-7224697 | Common:4; Rare:125; Clinvar:10; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
chr17:7234456-7234648 | Common:2; Rare:102 | ||||
chr17:7241400-7241680 | Rare:62 | ||||
chr17:7251963-7252314 | Common:1; Rare:137 | ||||
chr17:7281444-7281774 | Common:3; Rare:89 |