| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42609315-42609792 | Common:8; Rare:189; Clinvar (benign):2 | ||||
| chr17:42659114-42659426 | Rare:91 | ||||
| chr17:42675975-42676066 | Rare:16 | ||||
| chr17:42676806-42676873 | Common:1; Rare:13 | ||||
| chr17:42676915-42677027 | Rare:33 | ||||
| chr17:42677116-42677391 | Common:1; Rare:60 | ||||
| chr17:42682429-42682593 | Rare:38 | ||||
| chr17:42744357-42744812 | Common:1; Rare:97 | ||||
| chr17:42744888-42745234 | Common:3; Rare:119 | ||||
| chr17:42760680-42760845 | Common:5; Rare:53 | ||||
| chr17:42760961-42761191 | Rare:54 | ||||
| chr17:42761233-42761285 | Rare:18 | ||||
| chr17:42761289-42761443 | Common:2; Rare:34 | ||||
| chr17:42761451-42761522 | Common:1; Rare:17 | ||||
| chr17:42773264-42773528 | Rare:63 |