| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979103-75979283 | Rare:50; Clinvar:4 | ||||
| chr17:75979381-75979488 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr17:76027295-76027538 | Rare:54 | ||||
| chr17:76103712-76103867 | Common:4; Rare:49 | ||||
| chr17:76726467-76726882 | Common:5; Rare:156 | ||||
| chr17:76737328-76737487 | Common:2; Rare:61 | ||||
| chr17:76737901-76738121 | Common:3; Rare:65 | ||||
| chr17:78187042-78187365 | Common:3; Rare:102 | ||||
| chr17:78782255-78782572 | Common:9; Rare:105 | ||||
| chr17:78840751-78841037 | Common:2; Rare:103 | ||||
| chr17:80036556-80036652 | Common:2; Rare:27; Clinvar (benign):2 | ||||
| chr17:80220327-80220453 | Rare:50; Clinvar:1 | ||||
| chr17:80415105-80415184 | Common:1; Rare:51 | ||||
| chr17:81666567-81666763 | Common:1; Rare:86 | ||||
| chr17:81683699-81684057 | Common:4; Rare:177 |