| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75153418-75153531 | Rare:25 | ||||
| chr17:75154115-75154187 | Rare:25 | ||||
| chr17:75154392-75154836 | Common:1; Rare:145 | ||||
| chr17:75182497-75182733 | Common:3; Rare:73 | ||||
| chr17:75182845-75183278 | Common:2; Rare:138 | ||||
| chr17:75205159-75205769 | Common:2; Rare:197 | ||||
| chr17:75260868-75261272 | Common:5; Rare:93 | ||||
| chr17:75261305-75261450 | Rare:42 | ||||
| chr17:75261516-75262001 | Common:4; Rare:174; Clinvar (benign):4 | ||||
| chr17:75262109-75262193 | Common:1; Rare:21 | ||||
| chr17:75270490-75270867 | Rare:85 | ||||
| chr17:75271085-75271424 | Common:4; Rare:65 | ||||
| chr17:75288866-75289037 | Rare:31 | ||||
| chr17:75289157-75289296 | Common:1; Rare:28 | ||||
| chr17:75289326-75289742 | Common:3; Rare:132; Clinvar:1; Clinvar (benign):2 |