Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6444167-6444455 | Common:2; Rare:86 | ||||
chr17:6640646-6641089 | Common:7; Rare:138 | ||||
chr17:6651558-6651774 | Common:1; Rare:76 | ||||
chr17:7012315-7012686 | Rare:128 | ||||
chr17:7219828-7219938 | Common:3; Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
chr17:7241601-7241934 | Common:2; Rare:72 | ||||
chr17:7242239-7242564 | Common:1; Rare:104 | ||||
chr17:7251967-7252313 | Common:1; Rare:133 | ||||
chr17:7262405-7262615 | Rare:46 | ||||
chr17:7315042-7315437 | Common:4; Rare:141 | ||||
chr17:7352068-7352202 | Rare:44 | ||||
chr17:7484222-7484378 | Common:1; Rare:65 | ||||
chr17:7558111-7558309 | Common:1; Rare:34 | ||||
chr17:7583751-7583865 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7584074-7584113 | Rare:8 |