| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15999578-15999984 | Common:3; Rare:182; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:16040439-16040629 | Common:1; Rare:28 | ||||
| chr17:16217115-16217240 | Rare:37; Clinvar:1 | ||||
| chr17:17496377-17496607 | Common:3; Rare:63 | ||||
| chr17:18039155-18039430 | Common:5; Rare:74; Clinvar (benign):1 | ||||
| chr17:18253319-18253567 | Rare:91 | ||||
| chr17:18254547-18254823 | Rare:98 | ||||
| chr17:18314895-18315297 | Common:1; Rare:111 | ||||
| chr17:18781121-18781301 | Common:3; Rare:50 | ||||
| chr17:18856168-18856378 | Common:1; Rare:40 | ||||
| chr17:19362686-19362908 | Common:1; Rare:82 | ||||
| chr17:19378243-19378537 | Common:2; Rare:69 | ||||
| chr17:19387149-19387378 | Rare:58 | ||||
| chr17:19648657-19649063 | Common:3; Rare:150; Clinvar (benign):1 | ||||
| chr17:20155836-20156051 | Common:1; Rare:65 |