Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77390209-77390295 | Rare:18 | ||||
chr17:77433458-77433690 | Rare:52 | ||||
chr17:78416939-78417100 | Rare:35 | ||||
chr17:78862170-78862264 | Rare:20 | ||||
chr17:79027588-79027914 | Common:2; Rare:62 | ||||
chr17:80108309-80108509 | Common:1; Rare:72; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
chr17:80263422-80263775 | Rare:88 | ||||
chr17:80364404-80364463 | Rare:24; Clinvar:1 | ||||
chr17:80389697-80389872 | Common:1; Rare:52 | ||||
chr17:81260272-81260533 | Common:2; Rare:73 | ||||
chr17:81926619-81926668 | Rare:8 | ||||
chr17:82217717-82217965 | Rare:67 | ||||
chr18:3593962-3594219 | Common:3; Rare:41 | ||||
chr18:3594972-3595114 | Common:1; Rare:29 | ||||
chr18:3595557-3595637 | Rare:8 |