| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47693822-47694947 | Common:37; Rare:598 | ||||
| chr17:47694920-47695885 | Common:19; Rare:828 | ||||
| chr17:47821480-47822030 | Common:10; Rare:279 | ||||
| chr17:47831430-47831820 | Common:1; Rare:442 | ||||
| chr17:47840652-47841569 | Common:3; Rare:802 | ||||
| chr17:47850760-47851500 | Common:20; Rare:503 | ||||
| chr17:47895631-47896687 | Common:31; Rare:1419 | ||||
| chr17:47941244-47941802 | Rare:1025; Clinvar:49; Clinvar (benign):49; Clinvar (pathogenic):9 | ||||
| chr17:47941930-47942330 | Common:3; Rare:60 | ||||
| chr17:47970726-47971220 | Common:11; Rare:293 | ||||
| chr17:48047726-48047928 | Common:2; Rare:81 | ||||
| chr17:48047963-48048453 | Common:6; Rare:784 | ||||
| chr17:48048450-48048865 | Common:24; Rare:260 | ||||
| chr17:48048868-48049033 | Common:2; Rare:41 | ||||
| chr17:48048937-48049337 | Common:8; Rare:131 |