| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77373164-77373429 | Rare:93 | ||||
| chr17:77374433-77374653 | Rare:48 | ||||
| chr17:77450616-77450785 | Rare:34 | ||||
| chr17:78128708-78128821 | Common:6; Rare:28 | ||||
| chr17:78187041-78187372 | Common:3; Rare:105 | ||||
| chr17:78214109-78214328 | Common:3; Rare:74 | ||||
| chr17:78360185-78360501 | Common:2; Rare:84 | ||||
| chr17:78723556-78723693 | Rare:38 | ||||
| chr17:78782233-78782555 | Common:9; Rare:106 | ||||
| chr17:78840740-78841114 | Common:2; Rare:141 | ||||
| chr17:78979866-78980036 | Common:1; Rare:36 | ||||
| chr17:79009744-79009947 | Common:8; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:80035843-80035994 | Common:1; Rare:56 | ||||
| chr17:80036610-80036665 | Common:2; Rare:13; Clinvar (benign):2 | ||||
| chr17:80101366-80101668 | Common:5; Rare:132; Clinvar (benign):5 |