| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47831516-47831746 | Rare:63 | ||||
| chr17:47941356-47941719 | Rare:100; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970844-47971152 | Common:1; Rare:73 | ||||
| chr17:48048069-48048405 | Rare:86 | ||||
| chr17:48048602-48048826 | Common:4; Rare:33 | ||||
| chr17:48101376-48101561 | Common:2; Rare:60 | ||||
| chr17:48107670-48107806 | Common:1; Rare:32 | ||||
| chr17:48544716-48544761 | Common:2; Rare:16 | ||||
| chr17:48610763-48611082 | Common:4; Rare:86 | ||||
| chr17:48841521-48841686 | Common:2; Rare:17 | ||||
| chr17:48944765-48944918 | Common:2; Rare:53 | ||||
| chr17:49210581-49210712 | Rare:19 | ||||
| chr17:49788452-49788736 | Common:1; Rare:91 | ||||
| chr17:50192499-50192651 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:50194588-50194803 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 |