| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47649756-47650098 | Rare:142 | ||||
| chr17:47650244-47650417 | Rare:64 | ||||
| chr17:47650427-47650870 | Common:4; Rare:172 | ||||
| chr17:47693952-47694084 | Common:1; Rare:21 | ||||
| chr17:47694134-47694230 | Rare:13 | ||||
| chr17:47694600-47694651 | Rare:12 | ||||
| chr17:47694824-47694859 | Rare:7 | ||||
| chr17:47821681-47821867 | Common:3; Rare:43 | ||||
| chr17:47831318-47831704 | Common:1; Rare:120 | ||||
| chr17:47840861-47840973 | Common:1; Rare:28 | ||||
| chr17:47841189-47841499 | Rare:65 | ||||
| chr17:47850888-47851251 | Common:1; Rare:72 | ||||
| chr17:47895713-47896296 | Common:3; Rare:169 | ||||
| chr17:47896405-47896625 | Common:2; Rare:50 | ||||
| chr17:47941262-47941724 | Rare:125; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 |