| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:62064910-62065196 | Rare:168 | ||||
| chr17:62065229-62065423 | Common:5; Rare:94 | ||||
| chr17:62065685-62066011 | Common:3; Rare:103 | ||||
| chr17:62423717-62424041 | Common:3; Rare:292 | ||||
| chr17:62424301-62424930 | Common:5; Rare:207 | ||||
| chr17:62477785-62478218 | Common:3; Rare:256 | ||||
| chr17:62478444-62479042 | Common:12; Rare:455 | ||||
| chr17:62627497-62627990 | Common:3; Rare:257 | ||||
| chr17:62680750-62681070 | Common:1; Rare:114 | ||||
| chr17:62703700-62704180 | Common:12; Rare:248 | ||||
| chr17:62808040-62808560 | Common:10; Rare:336 | ||||
| chr17:63435806-63436573 | Common:5; Rare:392; Clinvar (pathogenic):2 | ||||
| chr17:63445585-63445964 | Common:5; Rare:154 | ||||
| chr17:63446008-63446487 | Common:3; Rare:381 | ||||
| chr17:63446650-63446960 | Common:11; Rare:166 |