| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7352081-7352207 | Rare:37 | ||||
| chr17:7438140-7438320 | Common:1; Rare:38 | ||||
| chr17:7440457-7440768 | Rare:61 | ||||
| chr17:7479517-7479809 | Common:3; Rare:49 | ||||
| chr17:7483911-7484051 | Common:5; Rare:31 | ||||
| chr17:7484188-7484371 | Common:1; Rare:74 | ||||
| chr17:7484690-7484834 | Rare:60 | ||||
| chr17:7583535-7583868 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584074-7584113 | Rare:8 | ||||
| chr17:7627469-7627551 | Common:1; Rare:20 | ||||
| chr17:7686412-7686688 | Rare:69 | ||||
| chr17:7687477-7687625 | Rare:31 | ||||
| chr17:7857382-7857718 | Common:3; Rare:108 | ||||
| chr17:7857909-7858074 | Rare:58 | ||||
| chr17:7885187-7885351 | Rare:51 |