| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698001-30698246 | Common:1; Rare:112 | ||||
| chr16:30698425-30698727 | Common:1; Rare:115 | ||||
| chr16:30698979-30699392 | Rare:113; Clinvar (benign):1 | ||||
| chr16:30748125-30748457 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762058-30762557 | Common:5; Rare:156 | ||||
| chr16:30787139-30787316 | Rare:31 | ||||
| chr16:30923053-30923107 | Rare:18 | ||||
| chr16:30923238-30923608 | Common:1; Rare:88 | ||||
| chr16:30957186-30957284 | Common:3; Rare:21 | ||||
| chr16:30996744-30997045 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:31010369-31010585 | Common:2; Rare:40 | ||||
| chr16:31033184-31033582 | Common:2; Rare:115 | ||||
| chr16:31072785-31073043 | Common:1; Rare:52 | ||||
| chr16:31073716-31073848 | Rare:41 | ||||
| chr16:31074149-31074473 | Common:2; Rare:94 |