| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30534828-30535105 | Common:3; Rare:89 | ||||
| chr16:30585687-30585925 | Common:1; Rare:47 | ||||
| chr16:30698455-30698580 | Rare:55 | ||||
| chr16:30762088-30762331 | Common:3; Rare:87 | ||||
| chr16:30787165-30787296 | Rare:21 | ||||
| chr16:30923256-30923585 | Common:1; Rare:79 | ||||
| chr16:31033460-31033592 | Common:1; Rare:51 | ||||
| chr16:31074184-31074438 | Common:1; Rare:68 | ||||
| chr16:31094598-31094836 | Common:1; Rare:91; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108291-31108458 | Rare:39 | ||||
| chr16:31179839-31180152 | Common:1; Rare:116 | ||||
| chr16:31442771-31443059 | Common:1; Rare:47 | ||||
| chr16:31472023-31472186 | Rare:42 | ||||
| chr16:31508389-31508484 | Common:2; Rare:36 | ||||
| chr16:46689134-46689293 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 |