| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41585127-41585357 | Rare:39 | ||||
| chr17:41586255-41586395 | Rare:34; Clinvar:1 | ||||
| chr17:41610513-41610986 | Common:2; Rare:128; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:41612116-41612161 | Rare:14 | ||||
| chr17:41619782-41620580 | Common:4; Rare:145 | ||||
| chr17:41620914-41621229 | Rare:94; Clinvar (pathogenic):1 | ||||
| chr17:41621255-41621278 | Rare:4 | ||||
| chr17:41621284-41621775 | Common:1; Rare:134 | ||||
| chr17:41628613-41629003 | Common:3; Rare:65 | ||||
| chr17:41651469-41651747 | Common:1; Rare:62 | ||||
| chr17:41654182-41654457 | Common:2; Rare:50 | ||||
| chr17:41655751-41656006 | Common:1; Rare:51 | ||||
| chr17:41663602-41663767 | Common:1; Rare:28 | ||||
| chr17:41665292-41665566 | Common:4; Rare:40 | ||||
| chr17:41665921-41666128 | Rare:51 |