Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:732319-732555 | Common:1; Rare:86 | ||||
chr17:752229-752357 | Common:2; Rare:48 | ||||
chr17:1400048-1400427 | Common:3; Rare:151 | ||||
chr17:1516567-1516952 | Common:1; Rare:138 | ||||
chr17:1684799-1685102 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
chr17:1716184-1716547 | Common:3; Rare:116 | ||||
chr17:1829780-1830116 | Common:9; Rare:139 | ||||
chr17:2303745-2303987 | Common:2; Rare:91 | ||||
chr17:2511886-2511992 | Common:1; Rare:29 | ||||
chr17:3636233-3636479 | Common:4; Rare:69; Clinvar (benign):1 | ||||
chr17:3668538-3668820 | Common:3; Rare:112 | ||||
chr17:3723773-3723907 | Common:1; Rare:75 | ||||
chr17:4142954-4143234 | Common:3; Rare:97 | ||||
chr17:4143612-4143748 | Common:4; Rare:79 | ||||
chr17:4263934-4264072 | Rare:56 |