| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16216171-16216807 | Common:3; Rare:138 | ||||
| chr17:16216830-16217380 | Rare:453; Clinvar:10; Clinvar (pathogenic):2 | ||||
| chr17:16352608-16353075 | Common:4; Rare:191 | ||||
| chr17:16353161-16353717 | Common:2; Rare:488 | ||||
| chr17:16380526-16380926 | Common:13; Rare:288 | ||||
| chr17:16380910-16381820 | Common:8; Rare:576 | ||||
| chr17:16414904-16415307 | Common:4; Rare:157 | ||||
| chr17:16415433-16415833 | Common:15; Rare:246 | ||||
| chr17:16419060-16419500 | Common:6; Rare:333 | ||||
| chr17:16491979-16492379 | Common:8; Rare:287 | ||||
| chr17:16653563-16654119 | Common:4; Rare:336 | ||||
| chr17:17041687-17042120 | Common:2; Rare:153 | ||||
| chr17:17042169-17042569 | Common:95; Rare:548 | ||||
| chr17:17205725-17206188 | Common:2; Rare:267 | ||||
| chr17:17206231-17206676 | Common:20; Rare:664 |