| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89948559-89948812 | Common:3; Rare:75 | ||||
| chr16:89972462-89972614 | Common:1; Rare:51 | ||||
| chr17:352795-352847 | Rare:9 | ||||
| chr17:386209-386405 | Common:3; Rare:45 | ||||
| chr17:410013-410430 | Common:9; Rare:192 | ||||
| chr17:714759-714953 | Common:3; Rare:62 | ||||
| chr17:732302-732639 | Common:2; Rare:122 | ||||
| chr17:752138-752360 | Common:2; Rare:89 | ||||
| chr17:1115388-1115616 | Rare:44 | ||||
| chr17:1400048-1400420 | Common:3; Rare:150 | ||||
| chr17:1516588-1516978 | Common:2; Rare:137 | ||||
| chr17:1684788-1685057 | Common:2; Rare:86; Clinvar:6; Clinvar (benign):1 | ||||
| chr17:1716245-1716536 | Common:3; Rare:85 | ||||
| chr17:1829786-1830082 | Common:8; Rare:126 | ||||
| chr17:2303444-2303659 | Rare:79 |