Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5078140-5078523 | Common:4; Rare:97 | ||||
chr17:5191838-5192106 | Common:2; Rare:88 | ||||
chr17:5234783-5234946 | Rare:43 | ||||
chr17:5419566-5419882 | Common:3; Rare:111 | ||||
chr17:5420066-5420213 | Rare:62 | ||||
chr17:5486149-5486399 | Common:4; Rare:108 | ||||
chr17:6640651-6641077 | Common:7; Rare:130 | ||||
chr17:6651574-6651662 | Common:1; Rare:25 | ||||
chr17:7012315-7012705 | Rare:131 | ||||
chr17:7219668-7219961 | Common:4; Rare:101; Clinvar:5; Clinvar (benign):2 | ||||
chr17:7221254-7221559 | Common:9; Rare:91; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:7221817-7222068 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
chr17:7251963-7252062 | Rare:42 | ||||
chr17:7315069-7315411 | Common:4; Rare:118 | ||||
chr17:7351601-7351856 | Common:1; Rare:59 |