| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636241-3636779 | Common:8; Rare:147; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:3668537-3668820 | Common:3; Rare:113 | ||||
| chr17:4142967-4143245 | Common:3; Rare:96 | ||||
| chr17:4143597-4143744 | Common:4; Rare:84 | ||||
| chr17:4263943-4264042 | Rare:43 | ||||
| chr17:4704092-4704239 | Rare:76 | ||||
| chr17:4736338-4736513 | Rare:35 | ||||
| chr17:4739376-4739441 | Common:1; Rare:25 | ||||
| chr17:4739542-4739683 | Common:1; Rare:38 | ||||
| chr17:4739739-4740015 | Common:2; Rare:61 | ||||
| chr17:4806996-4807192 | Common:4; Rare:65 | ||||
| chr17:4939887-4940333 | Common:2; Rare:133 | ||||
| chr17:4967733-4968060 | Common:1; Rare:116 | ||||
| chr17:4987625-4987819 | Common:2; Rare:67 | ||||
| chr17:4997884-4998154 | Common:2; Rare:107; Clinvar (benign):1 |