| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7221324-7221606 | Common:9; Rare:88; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:7224526-7224884 | Common:2; Rare:122; Clinvar:10; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr17:7239411-7239709 | Common:3; Rare:87 | ||||
| chr17:7242245-7242473 | Common:1; Rare:72 | ||||
| chr17:7251963-7252321 | Common:1; Rare:141 | ||||
| chr17:7261076-7261234 | Common:1; Rare:45 | ||||
| chr17:7262456-7262657 | Rare:47 | ||||
| chr17:7351630-7351738 | Rare:19 | ||||
| chr17:7352054-7352207 | Rare:48 | ||||
| chr17:7420204-7420342 | Common:1; Rare:21 | ||||
| chr17:7479479-7479713 | Common:1; Rare:40 | ||||
| chr17:7484215-7484381 | Common:1; Rare:69 | ||||
| chr17:7484505-7484777 | Common:2; Rare:107 | ||||
| chr17:7499161-7499392 | Common:2; Rare:59 | ||||
| chr17:7549006-7549242 | Common:3; Rare:54; Clinvar:1; Clinvar (benign):1 |