| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15999598-15999956 | Common:3; Rare:171; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr17:16039583-16039789 | Common:1; Rare:48 | ||||
| chr17:16215515-16215629 | Rare:49 | ||||
| chr17:16217118-16217249 | Rare:46; Clinvar:1 | ||||
| chr17:16380645-16381183 | Common:5; Rare:169 | ||||
| chr17:16415475-16415824 | Common:4; Rare:83 | ||||
| chr17:16569186-16569311 | Common:1; Rare:31 | ||||
| chr17:17281183-17281407 | Rare:87 | ||||
| chr17:17496378-17496546 | Rare:41 | ||||
| chr17:17591368-17591499 | Common:1; Rare:46 | ||||
| chr17:17591589-17591897 | Common:2; Rare:91 | ||||
| chr17:17819399-17819655 | Rare:82 | ||||
| chr17:17820413-17820663 | Common:1; Rare:51 | ||||
| chr17:17823532-17823816 | Common:5; Rare:137 | ||||
| chr17:18087693-18088024 | Rare:86 |