| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75153498-75154124 | Common:4; Rare:244 | ||||
| chr17:75154305-75155000 | Common:7; Rare:900 | ||||
| chr17:75154995-75155395 | Common:1; Rare:67 | ||||
| chr17:75182437-75182837 | Common:10; Rare:294 | ||||
| chr17:75182840-75183282 | Common:10; Rare:695 | ||||
| chr17:75205146-75206061 | Common:8; Rare:991 | ||||
| chr17:75240278-75240784 | Common:4; Rare:185 | ||||
| chr17:75260904-75261470 | Common:19; Rare:324 | ||||
| chr17:75261480-75261980 | Common:28; Rare:970; Clinvar (benign):21 | ||||
| chr17:75262249-75263363 | Common:16; Rare:456; Clinvar (benign):11 | ||||
| chr17:75270311-75270975 | Common:1; Rare:318 | ||||
| chr17:75271035-75271698 | Common:27; Rare:432 | ||||
| chr17:75288724-75289124 | Common:1; Rare:83 | ||||
| chr17:75289254-75290119 | Common:24; Rare:884; Clinvar:7; Clinvar (benign):12 | ||||
| chr17:75326251-75326651 | Common:1; Rare:99 |