| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7558206-7558331 | Rare:29 | ||||
| chr17:7558412-7558799 | Rare:78 | ||||
| chr17:7558895-7559027 | Common:1; Rare:29 | ||||
| chr17:7561784-7562003 | Common:2; Rare:61 | ||||
| chr17:7577056-7577391 | Common:1; Rare:87 | ||||
| chr17:7579559-7579925 | Common:1; Rare:132 | ||||
| chr17:7583530-7583885 | Common:1; Rare:143; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584068-7584308 | Common:1; Rare:54 | ||||
| chr17:7626943-7627904 | Common:4; Rare:291 | ||||
| chr17:7686392-7686688 | Rare:75 | ||||
| chr17:7687457-7687557 | Rare:25; Clinvar:1 | ||||
| chr17:7843642-7843733 | Rare:32 | ||||
| chr17:7857100-7858080 | Common:6; Rare:364 | ||||
| chr17:7885176-7885351 | Rare:57 | ||||
| chr17:7885517-7885786 | Common:4; Rare:61 |