| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:61863237-61863286 | Common:1; Rare:10; Clinvar (benign):1 | ||||
| chr17:61863287-61863362 | Rare:16; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:61863389-61863830 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:61863937-61864045 | Rare:19 | ||||
| chr17:61926991-61927289 | Rare:59 | ||||
| chr17:61927412-61927632 | Common:2; Rare:52 | ||||
| chr17:61927885-61928135 | Common:2; Rare:95 | ||||
| chr17:62064836-62064890 | Rare:24 | ||||
| chr17:62064917-62064966 | Rare:11 | ||||
| chr17:62065123-62065442 | Common:4; Rare:100 | ||||
| chr17:62065675-62066185 | Common:4; Rare:162 | ||||
| chr17:62423713-62424071 | Common:2; Rare:129 | ||||
| chr17:62424340-62424399 | Rare:13 | ||||
| chr17:62477913-62478227 | Common:2; Rare:90 | ||||
| chr17:62478425-62478473 | Rare:10 |