| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7012950-7013051 | Rare:17 | ||||
| chr17:7080235-7080583 | Common:1; Rare:49 | ||||
| chr17:7219725-7219944 | Common:3; Rare:87; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:7221240-7221637 | Common:9; Rare:117; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:7223307-7223369 | Rare:18 | ||||
| chr17:7224366-7224819 | Common:4; Rare:164; Clinvar:11; Clinvar (benign):22; Clinvar (pathogenic):3 | ||||
| chr17:7234357-7234628 | Common:1; Rare:126 | ||||
| chr17:7241784-7241934 | Common:2; Rare:33 | ||||
| chr17:7242246-7242262 | Rare:2 | ||||
| chr17:7251963-7252321 | Common:1; Rare:141 | ||||
| chr17:7261092-7261196 | Common:1; Rare:27 | ||||
| chr17:7262358-7262698 | Common:2; Rare:74 | ||||
| chr17:7263952-7264089 | Rare:23 | ||||
| chr17:7281420-7281752 | Common:2; Rare:89 | ||||
| chr17:7351594-7351722 | Rare:25 |