| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59846036-59846137 | Rare:10 | ||||
| chr17:59846344-59846455 | Rare:14 | ||||
| chr17:59847542-59847621 | Common:1; Rare:10 | ||||
| chr17:59847623-59847681 | Rare:8 | ||||
| chr17:59848902-59849063 | Common:2; Rare:28 | ||||
| chr17:60135518-60135820 | Rare:79 | ||||
| chr17:60150963-60151118 | Rare:23 | ||||
| chr17:60391009-60391401 | Rare:61 | ||||
| chr17:60577197-60577350 | Rare:27 | ||||
| chr17:60577665-60577706 | Common:1; Rare:7 | ||||
| chr17:60577723-60577818 | Rare:19 | ||||
| chr17:60600841-60600929 | Rare:18; Clinvar (benign):1 | ||||
| chr17:62064084-62064247 | Rare:32 | ||||
| chr17:62065832-62066175 | Common:2; Rare:117 | ||||
| chr17:62093600-62093740 | Rare:20 |