| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63602292-63602380 | Rare:9 | ||||
| chr17:63635063-63635198 | Rare:26 | ||||
| chr17:63670656-63670972 | Rare:43 | ||||
| chr17:63685548-63685624 | Rare:10 | ||||
| chr17:63701735-63702065 | Common:3; Rare:104 | ||||
| chr17:63762993-63763095 | Rare:21 | ||||
| chr17:63775294-63775593 | Common:2; Rare:72 | ||||
| chr17:63798016-63798404 | Rare:91 | ||||
| chr17:63820201-63820239 | Common:4; Rare:24 | ||||
| chr17:63820904-63821338 | Common:1; Rare:161 | ||||
| chr17:63825381-63825630 | Common:2; Rare:91 | ||||
| chr17:63931355-63931471 | Rare:34; Clinvar (benign):1 | ||||
| chr17:64005657-64005849 | Rare:29 | ||||
| chr17:64008154-64008246 | Rare:20 | ||||
| chr17:64010223-64010528 | Rare:44 |