Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5419585-5419876 | Common:3; Rare:101 | ||||
chr17:5420129-5420225 | Rare:38 | ||||
chr17:5486166-5486573 | Common:5; Rare:136 | ||||
chr17:5486796-5486916 | Common:4; Rare:35 | ||||
chr17:6640645-6641079 | Common:7; Rare:133 | ||||
chr17:6651574-6651714 | Common:1; Rare:48 | ||||
chr17:7012314-7012705 | Rare:131 | ||||
chr17:7219718-7219944 | Common:3; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr17:7234479-7234650 | Common:2; Rare:90 | ||||
chr17:7242255-7242589 | Common:1; Rare:107 | ||||
chr17:7251925-7252274 | Common:2; Rare:131 | ||||
chr17:7307888-7308027 | Common:1; Rare:35 | ||||
chr17:7351615-7351738 | Rare:23 | ||||
chr17:7352054-7352212 | Rare:51 | ||||
chr17:7479490-7479725 | Common:1; Rare:41 |