Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:74368137-74368379 | Common:1; Rare:67 | ||||
chr16:79598419-79598671 | Common:10; Rare:59 | ||||
chr17:3665010-3665180 | Common:2; Rare:23 | ||||
chr17:5499870-5500132 | Common:3; Rare:56 | ||||
chr17:7887535-7887821 | Rare:65 | ||||
chr17:16438680-16439018 | Rare:79 | ||||
chr17:17836159-17836412 | Common:2; Rare:67 | ||||
chr17:38452394-38452444 | Common:1; Rare:6 | ||||
chr17:40820383-40820680 | Common:1; Rare:95 | ||||
chr17:41518879-41519138 | Rare:38 | ||||
chr17:41620964-41621331 | Rare:87 | ||||
chr17:41758502-41758762 | Common:1; Rare:55; Clinvar:4; Clinvar (benign):2 | ||||
chr17:41769164-41769419 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:42422730-42422747 | Rare:7; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr17:43388301-43388385 | Rare:18 |