| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45161482-45161926 | Common:1; Rare:116 | ||||
| chr17:45262052-45262232 | Common:1; Rare:31 | ||||
| chr17:45316970-45317237 | Common:5; Rare:84 | ||||
| chr17:45396841-45397135 | Common:2; Rare:96 | ||||
| chr17:45490708-45490834 | Rare:49 | ||||
| chr17:45620198-45620358 | Rare:39 | ||||
| chr17:45844707-45844900 | Rare:38 | ||||
| chr17:45894269-45894572 | Common:3; Rare:90; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46039155-46039422 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):4 | ||||
| chr17:46193517-46193646 | Common:2; Rare:44 | ||||
| chr17:46193749-46194063 | Common:4; Rare:70 | ||||
| chr17:46225339-46225483 | Common:2; Rare:37 | ||||
| chr17:46923084-46923187 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47157042-47157317 | Common:7; Rare:83 | ||||
| chr17:47189202-47189453 | Common:1; Rare:72 |