| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44219029-44219253 | Rare:75 | ||||
| chr17:44219467-44219870 | Rare:143 | ||||
| chr17:44219911-44220221 | Common:5; Rare:101 | ||||
| chr17:44220475-44220668 | Common:3; Rare:75 | ||||
| chr17:44220819-44220934 | Rare:28 | ||||
| chr17:44220968-44221469 | Common:1; Rare:159 | ||||
| chr17:44221552-44221803 | Common:4; Rare:74 | ||||
| chr17:44222086-44222323 | Rare:50 | ||||
| chr17:44315060-44315189 | Common:2; Rare:33 | ||||
| chr17:44324278-44324410 | Common:2; Rare:44 | ||||
| chr17:44324635-44325024 | Common:4; Rare:123 | ||||
| chr17:44325317-44325514 | Common:3; Rare:40 | ||||
| chr17:44344996-44345356 | Common:1; Rare:80; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44363809-44364180 | Common:3; Rare:70 | ||||
| chr17:44385285-44385706 | Common:5; Rare:137; Clinvar:4 |