| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89641216-89641268 | Common:3; Rare:21 | ||||
| chr16:89833780-89834064 | Common:2; Rare:82 | ||||
| chr16:89860811-89860887 | Common:1; Rare:22 | ||||
| chr16:89869442-89869682 | Rare:89 | ||||
| chr17:245198-245287 | Rare:30 | ||||
| chr17:1057041-1057326 | Common:10; Rare:59 | ||||
| chr17:1108453-1108553 | Rare:19 | ||||
| chr17:1110132-1110374 | Rare:57 | ||||
| chr17:1538869-1539141 | Common:2; Rare:58 | ||||
| chr17:1561096-1561136 | Rare:13 | ||||
| chr17:1626436-1626521 | Rare:11 | ||||
| chr17:1681938-1682256 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1712507-1712573 | Rare:8 | ||||
| chr17:1714371-1714592 | Rare:39 | ||||
| chr17:3658181-3658247 | Rare:24 |