| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76353859-76353943 | Rare:37 | ||||
| chr17:76726464-76726893 | Common:5; Rare:164 | ||||
| chr17:76737240-76737518 | Common:4; Rare:137 | ||||
| chr17:76737887-76738084 | Common:3; Rare:57 | ||||
| chr17:78187035-78187380 | Common:3; Rare:114 | ||||
| chr17:78782255-78782603 | Common:9; Rare:109 | ||||
| chr17:78840735-78841124 | Common:2; Rare:145 | ||||
| chr17:79183453-79183534 | Common:1; Rare:19 | ||||
| chr17:80035849-80035980 | Common:1; Rare:49 | ||||
| chr17:80220309-80220459 | Common:1; Rare:58; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415115-80415184 | Common:1; Rare:43 | ||||
| chr17:80991806-80991916 | Common:1; Rare:45 | ||||
| chr17:81239036-81239182 | Common:2; Rare:46 | ||||
| chr17:81295278-81295380 | Common:1; Rare:20 | ||||
| chr17:81666552-81666779 | Common:1; Rare:102 |