| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45060987-45061341 | Common:2; Rare:95 | ||||
| chr17:45148142-45148631 | Common:1; Rare:163 | ||||
| chr17:45160589-45160921 | Common:1; Rare:87 | ||||
| chr17:45161456-45161939 | Common:1; Rare:126 | ||||
| chr17:45490712-45490888 | Rare:60 | ||||
| chr17:45894247-45894594 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46045787-46045984 | Common:2; Rare:41 | ||||
| chr17:46192817-46193021 | Common:1; Rare:51 | ||||
| chr17:46225349-46225496 | Common:2; Rare:41 | ||||
| chr17:46922847-46923199 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):7 | ||||
| chr17:47189181-47189629 | Common:1; Rare:122 | ||||
| chr17:47323903-47324028 | Common:1; Rare:41 | ||||
| chr17:47649420-47649965 | Common:2; Rare:188 | ||||
| chr17:47693807-47694091 | Common:1; Rare:46 | ||||
| chr17:47831501-47831674 | Rare:49 |