| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59154858-59154994 | Rare:40 | ||||
| chr17:59155091-59155255 | Common:1; Rare:55 | ||||
| chr17:59155533-59155850 | Rare:79 | ||||
| chr17:59209924-59210160 | Common:1; Rare:87 | ||||
| chr17:59220366-59220796 | Common:4; Rare:126 | ||||
| chr17:59220901-59221165 | Rare:57 | ||||
| chr17:59331458-59332038 | Common:2; Rare:192 | ||||
| chr17:59565460-59565695 | Common:1; Rare:89 | ||||
| chr17:59566113-59566231 | Rare:28 | ||||
| chr17:59619111-59619447 | Common:4; Rare:91 | ||||
| chr17:59619473-59620024 | Common:3; Rare:186 | ||||
| chr17:59706400-59706713 | Common:3; Rare:66 | ||||
| chr17:59707368-59707787 | Common:4; Rare:107; Clinvar (benign):6 | ||||
| chr17:59707891-59707969 | Common:1; Rare:15 | ||||
| chr17:59836983-59837288 | Common:1; Rare:48 |