Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:752787-752902 | Rare:28 | ||||
chr17:1467838-1468153 | Common:2; Rare:129; Clinvar (benign):5 | ||||
chr17:1480588-1480878 | Common:2; Rare:96; Clinvar (benign):1 | ||||
chr17:1492604-1492707 | Rare:14 | ||||
chr17:1516582-1516958 | Common:2; Rare:133 | ||||
chr17:1716179-1716520 | Common:2; Rare:104 | ||||
chr17:1829842-1830039 | Common:6; Rare:81 | ||||
chr17:2029987-2030166 | Common:1; Rare:63 | ||||
chr17:2303734-2303987 | Common:2; Rare:95 | ||||
chr17:2336435-2336484 | Rare:14 | ||||
chr17:2593464-2593664 | Common:2; Rare:77 | ||||
chr17:2711762-2712031 | Common:2; Rare:75 | ||||
chr17:3636241-3636502 | Common:4; Rare:74; Clinvar (benign):1 | ||||
chr17:3668533-3668837 | Common:3; Rare:122 | ||||
chr17:3723764-3723917 | Common:1; Rare:84 |