| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59619197-59619452 | Common:4; Rare:69 | ||||
| chr17:59619469-59620011 | Common:3; Rare:185 | ||||
| chr17:59707353-59707787 | Common:4; Rare:110; Clinvar (benign):6 | ||||
| chr17:59837455-59838038 | Common:1; Rare:82 | ||||
| chr17:59892655-59892770 | Rare:24 | ||||
| chr17:59892783-59893242 | Common:1; Rare:137 | ||||
| chr17:59964278-59964503 | Rare:36 | ||||
| chr17:59964663-59964903 | Common:2; Rare:97 | ||||
| chr17:60078785-60079094 | Common:6; Rare:124 | ||||
| chr17:60305237-60305391 | Rare:40 | ||||
| chr17:60392031-60392264 | Common:2; Rare:55 | ||||
| chr17:60392318-60392631 | Common:2; Rare:100 | ||||
| chr17:60421638-60421769 | Rare:34 | ||||
| chr17:60525582-60525824 | Common:3; Rare:77 | ||||
| chr17:60525829-60526061 | Common:2; Rare:78 |