| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47840833-47841094 | Common:1; Rare:72 | ||||
| chr17:47841104-47841477 | Rare:82 | ||||
| chr17:47850906-47851035 | Rare:21 | ||||
| chr17:47851036-47851467 | Common:3; Rare:89 | ||||
| chr17:47895705-47896119 | Common:4; Rare:115 | ||||
| chr17:47896156-47896317 | Common:1; Rare:53 | ||||
| chr17:47896404-47896634 | Common:2; Rare:51 | ||||
| chr17:47896638-47896656 | Rare:4 | ||||
| chr17:47941262-47941889 | Rare:163; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr17:47957712-47958041 | Common:2; Rare:57 | ||||
| chr17:47958282-47958314 | Rare:7 | ||||
| chr17:47970751-47971225 | Common:4; Rare:123 | ||||
| chr17:47971242-47971504 | Common:1; Rare:89 | ||||
| chr17:48037717-48037817 | Common:1; Rare:27 | ||||
| chr17:48047715-48048451 | Common:2; Rare:202 |