| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4939892-4940391 | Common:2; Rare:147 | ||||
| chr17:4943375-4943477 | Common:1; Rare:44 | ||||
| chr17:4946627-4947052 | Common:2; Rare:101 | ||||
| chr17:4947900-4948013 | Rare:29 | ||||
| chr17:4948144-4948710 | Common:4; Rare:207 | ||||
| chr17:4948942-4949184 | Common:2; Rare:83 | ||||
| chr17:4967168-4967630 | Common:3; Rare:125 | ||||
| chr17:4967748-4967910 | Rare:67 | ||||
| chr17:4973199-4973469 | Common:1; Rare:62 | ||||
| chr17:4987394-4987819 | Common:4; Rare:134 | ||||
| chr17:4997892-4998154 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr17:5077991-5078304 | Common:2; Rare:69 | ||||
| chr17:5078363-5078523 | Common:4; Rare:50 | ||||
| chr17:5191831-5192106 | Common:2; Rare:89 | ||||
| chr17:5234739-5235001 | Rare:65 |