| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87948145-87948334 | Common:2; Rare:39 | ||||
| chr16:87956373-87956620 | Common:1; Rare:71 | ||||
| chr16:88046147-88046307 | Common:2; Rare:45 | ||||
| chr16:88069488-88069715 | Common:1; Rare:60 | ||||
| chr16:88430296-88430374 | Rare:22; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:88430377-88430469 | Common:1; Rare:27; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:88430576-88431039 | Common:4; Rare:174; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr16:88454646-88454897 | Rare:60 | ||||
| chr16:88455408-88455580 | Common:3; Rare:40 | ||||
| chr16:88456042-88456319 | Common:2; Rare:61 | ||||
| chr16:88456356-88456457 | Common:1; Rare:21 | ||||
| chr16:88465100-88465274 | Common:2; Rare:44 | ||||
| chr16:88534179-88534438 | Common:1; Rare:121 | ||||
| chr16:88634020-88634368 | Common:1; Rare:83 | ||||
| chr16:88634805-88635000 | Common:1; Rare:52 |