| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7234472-7234653 | Common:2; Rare:99 | ||||
| chr17:7251963-7252321 | Common:1; Rare:141 | ||||
| chr17:7281582-7281771 | Common:1; Rare:52 | ||||
| chr17:7351619-7351743 | Rare:23 | ||||
| chr17:7352065-7352206 | Rare:46 | ||||
| chr17:7479502-7479725 | Common:1; Rare:40 | ||||
| chr17:7484193-7484380 | Common:1; Rare:79 | ||||
| chr17:7503447-7503688 | Rare:71 | ||||
| chr17:7548978-7549237 | Common:3; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558206-7558309 | Rare:22 | ||||
| chr17:7558812-7559055 | Common:1; Rare:54 | ||||
| chr17:7573238-7573536 | Common:4; Rare:99 | ||||
| chr17:7583535-7583858 | Common:1; Rare:131; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7627799-7627990 | Common:2; Rare:61 | ||||
| chr17:7686412-7686677 | Rare:65 |