| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47100240-47100422 | Common:1; Rare:51 | ||||
| chr17:47417753-47417850 | Rare:21 | ||||
| chr17:47424010-47424145 | Rare:27 | ||||
| chr17:47437005-47437128 | Common:1; Rare:19 | ||||
| chr17:47438341-47438463 | Common:1; Rare:20 | ||||
| chr17:47446869-47447023 | Common:3; Rare:27 | ||||
| chr17:47492419-47492626 | Common:3; Rare:68 | ||||
| chr17:47621602-47621850 | Rare:47 | ||||
| chr17:47678211-47678421 | Common:1; Rare:31 | ||||
| chr17:47944408-47944640 | Common:1; Rare:54; Clinvar (pathogenic):1 | ||||
| chr17:47953223-47953516 | Common:4; Rare:70 | ||||
| chr17:48056923-48057080 | Rare:33 | ||||
| chr17:48076238-48076298 | Rare:8 | ||||
| chr17:48076874-48077271 | Rare:72 | ||||
| chr17:48546479-48546680 | Rare:37 |