| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699451-15699789 | Common:7; Rare:154 | ||||
| chr17:15944896-15945317 | Common:6; Rare:201 | ||||
| chr17:15999570-15999892 | Common:6; Rare:316; Clinvar:10; Clinvar (benign):16; Clinvar (pathogenic):4 | ||||
| chr17:16215464-16215675 | Common:3; Rare:154 | ||||
| chr17:16217056-16217287 | Rare:132; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr17:16313390-16313840 | Common:2; Rare:167; Clinvar:8; Clinvar (pathogenic):2 | ||||
| chr17:16353383-16353570 | Rare:123 | ||||
| chr17:16380996-16381360 | Common:4; Rare:147 | ||||
| chr17:17042104-17042539 | Common:20; Rare:152 | ||||
| chr17:17206102-17206900 | Common:8; Rare:390 | ||||
| chr17:17237133-17237707 | Common:15; Rare:245; Clinvar (benign):2 | ||||
| chr17:17281184-17281370 | Rare:144 | ||||
| chr17:17303262-17303393 | Common:2; Rare:95 | ||||
| chr17:17591297-17591503 | Common:1; Rare:86 | ||||
| chr17:17591589-17591960 | Common:4; Rare:204 |