| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32877028-32877393 | Rare:159 | ||||
| chr17:32927963-32928363 | Common:1; Rare:160 | ||||
| chr17:34255065-34255326 | Rare:64 | ||||
| chr17:34961190-34961651 | Common:9; Rare:370 | ||||
| chr17:34980342-34980882 | Common:15; Rare:343 | ||||
| chr17:34981069-34981287 | Common:4; Rare:75 | ||||
| chr17:35063632-35063836 | Rare:62 | ||||
| chr17:35088640-35089030 | Common:1; Rare:71 | ||||
| chr17:35089179-35089582 | Common:13; Rare:203 | ||||
| chr17:35119596-35120023 | Common:1; Rare:319; Clinvar:18; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:35142151-35142318 | Common:1; Rare:63 | ||||
| chr17:35242881-35243281 | Rare:253 | ||||
| chr17:35372859-35373197 | Common:3; Rare:65 | ||||
| chr17:35373129-35373623 | Common:8; Rare:110 | ||||
| chr17:35373546-35373851 | Common:6; Rare:63 |