| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44186658-44187002 | Common:1; Rare:127 | ||||
| chr17:44187161-44187274 | Rare:31 | ||||
| chr17:44220793-44220932 | Rare:37 | ||||
| chr17:44221219-44221367 | Rare:43 | ||||
| chr17:44324760-44325003 | Common:2; Rare:87 | ||||
| chr17:44503366-44503714 | Rare:134 | ||||
| chr17:44899379-44899741 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45060964-45061343 | Common:2; Rare:101 | ||||
| chr17:45132340-45132631 | Common:2; Rare:87 | ||||
| chr17:45148159-45148478 | Common:1; Rare:93 | ||||
| chr17:45161494-45161906 | Common:1; Rare:109 | ||||
| chr17:45490708-45490888 | Rare:61 | ||||
| chr17:46192838-46193134 | Common:3; Rare:72 | ||||
| chr17:46193351-46193613 | Common:4; Rare:72 | ||||
| chr17:46225353-46225480 | Common:1; Rare:33 |