| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75271132-75271386 | Common:3; Rare:48 | ||||
| chr17:75289372-75289709 | Common:3; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75456436-75456656 | Common:1; Rare:62 | ||||
| chr17:75525483-75525720 | Common:2; Rare:73 | ||||
| chr17:75667120-75667381 | Common:4; Rare:85 | ||||
| chr17:75779022-75779294 | Common:2; Rare:113 | ||||
| chr17:75844237-75844487 | Common:1; Rare:75; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:75855290-75855658 | Common:1; Rare:100 | ||||
| chr17:75979132-75979626 | Common:1; Rare:138; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:76103688-76103895 | Common:6; Rare:72 | ||||
| chr17:76264872-76265237 | Common:1; Rare:97 | ||||
| chr17:76481889-76481931 | Common:1; Rare:10 | ||||
| chr17:76726424-76727041 | Common:5; Rare:235 | ||||
| chr17:76737327-76737691 | Common:3; Rare:123 | ||||
| chr17:76737861-76738054 | Common:3; Rare:54 |