| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75393754-75394066 | Common:1; Rare:67 | ||||
| chr17:75456465-75456729 | Rare:81 | ||||
| chr17:75588353-75588434 | Common:1; Rare:24 | ||||
| chr17:75667136-75667442 | Common:4; Rare:101 | ||||
| chr17:75784564-75784872 | Common:2; Rare:136 | ||||
| chr17:75855283-75855643 | Common:1; Rare:95 | ||||
| chr17:75904871-75904976 | Common:1; Rare:36 | ||||
| chr17:75979103-75979283 | Rare:50; Clinvar:4 | ||||
| chr17:75979381-75979478 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chr17:76072497-76072669 | Rare:51 | ||||
| chr17:76103696-76103876 | Common:5; Rare:64 | ||||
| chr17:76141251-76141419 | Common:1; Rare:46 | ||||
| chr17:76353585-76353671 | Rare:36 | ||||
| chr17:76353864-76354209 | Common:1; Rare:106 | ||||
| chr17:76501413-76501566 | Rare:44; Clinvar (benign):2 |