| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:60391839-60392820 | Common:12; Rare:691 | ||||
| chr17:60525600-60526514 | Common:14; Rare:787 | ||||
| chr17:60599510-60600520 | Common:11; Rare:727 | ||||
| chr17:60677251-60677530 | Common:3; Rare:151 | ||||
| chr17:60677627-60678107 | Common:3; Rare:264 | ||||
| chr17:60887475-60887694 | Common:1; Rare:41 | ||||
| chr17:61244910-61245490 | Common:2; Rare:151 | ||||
| chr17:61376826-61377741 | Common:11; Rare:207 | ||||
| chr17:61387844-61388739 | Common:8; Rare:292 | ||||
| chr17:61399208-61400084 | Common:2; Rare:235 | ||||
| chr17:61400156-61400599 | Common:2; Rare:252; Clinvar (pathogenic):2 | ||||
| chr17:61862796-61863842 | Common:12; Rare:472; Clinvar:8; Clinvar (benign):9 | ||||
| chr17:61863854-61864123 | Common:1; Rare:33 | ||||
| chr17:61927260-61927663 | Common:5; Rare:189 | ||||
| chr17:61927790-61928140 | Common:5; Rare:240 |