| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1684792-1685021 | Common:2; Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716198-1716536 | Common:3; Rare:103 | ||||
| chr17:1829786-1830051 | Common:8; Rare:112 | ||||
| chr17:2303293-2303375 | Rare:22 | ||||
| chr17:2303460-2303640 | Rare:66 | ||||
| chr17:2303722-2303980 | Common:2; Rare:100 | ||||
| chr17:2593863-2594001 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:3636241-3636496 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr17:3668532-3668877 | Common:3; Rare:139 | ||||
| chr17:3723767-3723932 | Common:1; Rare:96 | ||||
| chr17:4142987-4143244 | Rare:89 | ||||
| chr17:4143597-4143777 | Common:5; Rare:108 | ||||
| chr17:4263937-4264042 | Rare:46 | ||||
| chr17:4704108-4704266 | Rare:82 | ||||
| chr17:4731268-4731481 | Common:2; Rare:62 |