| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68955307-68955471 | Rare:33 | ||||
| chr17:69060902-69061125 | Common:1; Rare:36 | ||||
| chr17:69327069-69327371 | Common:2; Rare:101 | ||||
| chr17:69414615-69414759 | Rare:30 | ||||
| chr17:70169343-70169539 | Common:1; Rare:52 | ||||
| chr17:72120793-72121025 | Rare:60 | ||||
| chr17:72992913-72993076 | Common:1; Rare:32 | ||||
| chr17:73192817-73193067 | Common:15; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232100-73232722 | Common:4; Rare:237 | ||||
| chr17:73311982-73312105 | Rare:35 | ||||
| chr17:74213275-74213583 | Common:4; Rare:65 | ||||
| chr17:74748414-74748640 | Common:2; Rare:78 | ||||
| chr17:74776250-74776550 | Common:4; Rare:98 | ||||
| chr17:74873267-74873507 | Common:4; Rare:83 | ||||
| chr17:75012576-75012700 | Common:1; Rare:32 |