Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75876089-75876451 | Rare:106 | ||||
chr17:75877894-75878085 | Common:3; Rare:49 | ||||
chr17:75878537-75878787 | Common:3; Rare:79 | ||||
chr17:75878923-75878984 | Common:1; Rare:11 | ||||
chr17:75896412-75896626 | Common:2; Rare:41 | ||||
chr17:75896722-75897036 | Common:1; Rare:111 | ||||
chr17:75904813-75905048 | Common:4; Rare:77 | ||||
chr17:75905091-75905296 | Common:1; Rare:45 | ||||
chr17:75940954-75941237 | Common:1; Rare:90 | ||||
chr17:75978964-75979307 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr17:75979337-75979702 | Common:1; Rare:108; Clinvar (benign):1 | ||||
chr17:76072419-76072837 | Common:3; Rare:157 | ||||
chr17:76103679-76103964 | Common:6; Rare:94 | ||||
chr17:76121543-76121686 | Common:2; Rare:33 | ||||
chr17:76240424-76240921 | Common:6; Rare:154 |