| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:90019310-90019738 | Common:10; Rare:200 | ||||
| chr16:90019710-90020070 | Common:2; Rare:208 | ||||
| chr16:90022527-90022727 | Common:1; Rare:143 | ||||
| chr17:409940-410540 | Common:19; Rare:422 | ||||
| chr17:714707-714983 | Common:7; Rare:161; Clinvar (benign):1 | ||||
| chr17:732302-732647 | Common:4; Rare:237 | ||||
| chr17:752105-752378 | Common:5; Rare:203 | ||||
| chr17:781991-782829 | Common:10; Rare:852 | ||||
| chr17:979690-980060 | Common:7; Rare:308 | ||||
| chr17:996560-997418 | Common:3; Rare:359 | ||||
| chr17:1109048-1109226 | Common:1; Rare:108 | ||||
| chr17:1400054-1400358 | Common:5; Rare:212 | ||||
| chr17:1456180-1456491 | Common:8; Rare:228 | ||||
| chr17:1485720-1486083 | Common:8; Rare:233 | ||||
| chr17:1486774-1487320 | Common:3; Rare:222 |