Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4948914-4949185 | Common:2; Rare:92 | ||||
chr17:4967797-4967976 | Rare:69 | ||||
chr17:4987629-4987718 | Common:1; Rare:37 | ||||
chr17:5191837-5192090 | Common:1; Rare:81 | ||||
chr17:5419651-5419866 | Common:3; Rare:63 | ||||
chr17:5420054-5420210 | Rare:62 | ||||
chr17:5486127-5486589 | Common:6; Rare:165 | ||||
chr17:5486773-5486933 | Common:4; Rare:52 | ||||
chr17:6640400-6641107 | Common:9; Rare:202 | ||||
chr17:6651539-6651747 | Common:1; Rare:71 | ||||
chr17:7012301-7012727 | Rare:139 | ||||
chr17:7035796-7036083 | Rare:68 | ||||
chr17:7219745-7219984 | Common:3; Rare:98; Clinvar:6; Clinvar (benign):2 | ||||
chr17:7219991-7220192 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr17:7223647-7223863 | Rare:61; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):5 |