| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47941374-47941712 | Rare:93; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048069-48048405 | Rare:86 | ||||
| chr17:48048599-48048833 | Common:4; Rare:38 | ||||
| chr17:48101369-48101577 | Common:2; Rare:68 | ||||
| chr17:48107465-48107792 | Common:5; Rare:75 | ||||
| chr17:48544572-48544684 | Rare:62 | ||||
| chr17:48590239-48590428 | Common:1; Rare:42 | ||||
| chr17:48594157-48594310 | Rare:29 | ||||
| chr17:48610531-48610695 | Common:1; Rare:55 | ||||
| chr17:48944679-48944928 | Common:2; Rare:81 | ||||
| chr17:48997125-48997477 | Rare:67 | ||||
| chr17:49210166-49210432 | Common:2; Rare:40 | ||||
| chr17:49210591-49210712 | Rare:19 | ||||
| chr17:49414845-49415143 | Common:2; Rare:74 | ||||
| chr17:49708155-49708379 | Common:1; Rare:72 |