| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47831507-47831646 | Rare:37 | ||||
| chr17:47941341-47941732 | Rare:106; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048552-48048813 | Common:4; Rare:51 | ||||
| chr17:48107427-48107599 | Common:3; Rare:41 | ||||
| chr17:48544716-48544941 | Common:2; Rare:73 | ||||
| chr17:48729004-48729247 | Rare:48 | ||||
| chr17:48944773-48944888 | Common:1; Rare:38 | ||||
| chr17:49210459-49210721 | Common:1; Rare:46 | ||||
| chr17:49788556-49788736 | Common:1; Rare:58 | ||||
| chr17:50373168-50373235 | Common:2; Rare:28 | ||||
| chr17:50719450-50719792 | Common:1; Rare:122 | ||||
| chr17:50866340-50866774 | Common:3; Rare:121 | ||||
| chr17:51166336-51166501 | Common:2; Rare:37 | ||||
| chr17:51260134-51260802 | Common:4; Rare:284 | ||||
| chr17:54968570-54968814 | Common:3; Rare:108 |