| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63842623-63842858 | Rare:51 | ||||
| chr17:63842880-63843267 | Common:2; Rare:94 | ||||
| chr17:63932211-63932368 | Rare:47 | ||||
| chr17:64020085-64020434 | Common:1; Rare:66 | ||||
| chr17:64020524-64020798 | Common:2; Rare:49 | ||||
| chr17:64130027-64130424 | Common:7; Rare:104 | ||||
| chr17:64130564-64130996 | Rare:78 | ||||
| chr17:64263212-64263520 | Common:2; Rare:108 | ||||
| chr17:64496722-64496845 | Rare:47; Clinvar (benign):1 | ||||
| chr17:64496913-64497231 | Common:3; Rare:149; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:64505480-64505658 | Rare:50 | ||||
| chr17:64506173-64506464 | Common:5; Rare:130 | ||||
| chr17:64506717-64507103 | Common:3; Rare:165 | ||||
| chr17:64662245-64662469 | Common:2; Rare:115 | ||||
| chr17:64918979-64919036 | Common:1; Rare:22 |