| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75515466-75515644 | Common:3; Rare:52 | ||||
| chr17:75667127-75667441 | Common:4; Rare:105 | ||||
| chr17:75779746-75780123 | Common:1; Rare:137 | ||||
| chr17:75784586-75784872 | Common:2; Rare:125 | ||||
| chr17:75855272-75855639 | Common:1; Rare:101 | ||||
| chr17:75904847-75905020 | Common:3; Rare:61 | ||||
| chr17:75979081-75979283 | Rare:55; Clinvar:4 | ||||
| chr17:76103673-76103882 | Common:6; Rare:74 | ||||
| chr17:76141242-76141419 | Common:1; Rare:48 | ||||
| chr17:76353612-76353676 | Rare:27 | ||||
| chr17:76353858-76354231 | Common:1; Rare:114 | ||||
| chr17:76501385-76501566 | Rare:61; Clinvar (benign):3 | ||||
| chr17:76726454-76726886 | Common:5; Rare:165 | ||||
| chr17:76737308-76737537 | Common:3; Rare:92 | ||||
| chr17:76737831-76738084 | Common:3; Rare:74 |