| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31033434-31033617 | Common:1; Rare:68 | ||||
| chr16:31073709-31073848 | Rare:45 | ||||
| chr16:31074184-31074450 | Common:1; Rare:73 | ||||
| chr16:31459353-31459510 | Common:1; Rare:64 | ||||
| chr16:31472109-31472191 | Rare:23 | ||||
| chr16:31508369-31508508 | Common:4; Rare:58 | ||||
| chr16:31873633-31873862 | Rare:77 | ||||
| chr16:32254052-32254226 | Common:2; Rare:26 | ||||
| chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689521-46689720 | Common:2; Rare:85; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973577-46973789 | Rare:93 | ||||
| chr16:47461027-47461362 | Common:2; Rare:125; Clinvar (benign):2 | ||||
| chr16:48244244-48244383 | Common:2; Rare:48 | ||||
| chr16:50266500-50266573 | Common:1; Rare:20 | ||||
| chr16:53054907-53055058 | Common:1; Rare:29 |