| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979081-75979277 | Rare:53; Clinvar:4 | ||||
| chr17:75979358-75979510 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr17:76011866-76011923 | Rare:18 | ||||
| chr17:76353618-76353867 | Common:2; Rare:90 | ||||
| chr17:76726487-76726886 | Common:5; Rare:149 | ||||
| chr17:76737281-76737485 | Common:4; Rare:95 | ||||
| chr17:76737883-76738050 | Common:3; Rare:47 | ||||
| chr17:77140661-77141034 | Common:2; Rare:132 | ||||
| chr17:78187052-78187391 | Common:3; Rare:110 | ||||
| chr17:78782224-78782554 | Common:9; Rare:105 | ||||
| chr17:78840747-78841104 | Common:2; Rare:133 | ||||
| chr17:80035861-80035972 | Common:1; Rare:41 | ||||
| chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415105-80415189 | Common:1; Rare:56 | ||||
| chr17:81087218-81087549 | Common:2; Rare:93 |