| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32127380-32127890 | Common:4; Rare:159 | ||||
| chr17:32519052-32519744 | Common:5; Rare:370 | ||||
| chr17:32876337-32876560 | Common:1; Rare:70 | ||||
| chr17:32912297-32912601 | Common:2; Rare:55 | ||||
| chr17:33509454-33509601 | Common:2; Rare:27 | ||||
| chr17:34040316-34040443 | Common:1; Rare:25 | ||||
| chr17:34252410-34252790 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr17:34578920-34579580 | Common:4; Rare:225 | ||||
| chr17:34613140-34613540 | Common:13; Rare:164 | ||||
| chr17:34674360-34674910 | Common:6; Rare:111 | ||||
| chr17:34917430-34917750 | Rare:50 | ||||
| chr17:35151147-35151280 | Common:2; Rare:51 | ||||
| chr17:35286160-35286580 | Common:2; Rare:58 | ||||
| chr17:35567852-35568222 | Common:5; Rare:232 | ||||
| chr17:35568470-35568870 | Common:2; Rare:74 |