| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30355219-30355370 | Common:1; Rare:59 | ||||
| chr16:30698452-30698598 | Common:1; Rare:62 | ||||
| chr16:30748134-30748441 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762103-30762342 | Common:3; Rare:83 | ||||
| chr16:30893940-30894261 | Common:5; Rare:87 | ||||
| chr16:31033440-31033581 | Common:1; Rare:56 | ||||
| chr16:31074197-31074450 | Common:1; Rare:71 | ||||
| chr16:31202662-31202918 | Common:2; Rare:92 | ||||
| chr16:31459319-31459510 | Common:1; Rare:81 | ||||
| chr16:31472109-31472198 | Rare:26 | ||||
| chr16:31508389-31508478 | Common:1; Rare:34 | ||||
| chr16:46689130-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46831102-46831320 | Common:2; Rare:83 | ||||
| chr16:47461032-47461353 | Common:2; Rare:117; Clinvar (benign):2 | ||||
| chr16:53703814-53704203 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):2 |