| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16001163-16001193 | Common:1; Rare:5 | ||||
| chr17:16001673-16001955 | Common:4; Rare:55; Clinvar (benign):1 | ||||
| chr17:16006484-16006768 | Common:1; Rare:61; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:16007484-16008065 | Common:2; Rare:80 | ||||
| chr17:16008897-16009198 | Common:1; Rare:53 | ||||
| chr17:16014060-16014386 | Common:1; Rare:59 | ||||
| chr17:16017478-16017731 | Common:1; Rare:47 | ||||
| chr17:16019365-16019593 | Common:1; Rare:41 | ||||
| chr17:16019746-16020033 | Common:1; Rare:36 | ||||
| chr17:16020637-16020844 | Common:1; Rare:34 | ||||
| chr17:16021416-16021451 | Rare:9 | ||||
| chr17:16022387-16022569 | Common:2; Rare:39 | ||||
| chr17:16022864-16023061 | Common:4; Rare:33 | ||||
| chr17:16048098-16048365 | Common:1; Rare:51 | ||||
| chr17:16051587-16051682 | Common:2; Rare:17 |