| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30787080-30787328 | Rare:109 | ||||
| chr16:30893945-30894232 | Common:13; Rare:205 | ||||
| chr16:30896420-30896645 | Common:2; Rare:52 | ||||
| chr16:30922466-30922926 | Common:5; Rare:345 | ||||
| chr16:30922991-30923673 | Common:3; Rare:429 | ||||
| chr16:30948962-30950177 | Common:6; Rare:638 | ||||
| chr16:30957133-30957346 | Common:9; Rare:107 | ||||
| chr16:30957576-30958321 | Common:7; Rare:530 | ||||
| chr16:30985310-30986068 | Common:8; Rare:391; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr16:30996900-30997447 | Common:4; Rare:235; Clinvar:1; Clinvar (benign):6 | ||||
| chr16:31032520-31032760 | Rare:69 | ||||
| chr16:31032737-31033137 | Common:3; Rare:164 | ||||
| chr16:31033093-31033806 | Common:6; Rare:432 | ||||
| chr16:31072413-31072818 | Rare:102 | ||||
| chr16:31073163-31073536 | Common:4; Rare:183 |