| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87317394-87317511 | Common:2; Rare:43 | ||||
| chr16:87765901-87766033 | Rare:53 | ||||
| chr16:88570174-88570482 | Common:1; Rare:118 | ||||
| chr16:88663078-88663362 | Common:7; Rare:115 | ||||
| chr16:88706202-88706522 | Common:4; Rare:139 | ||||
| chr16:88716585-88716863 | Common:3; Rare:121; Clinvar (benign):1 | ||||
| chr16:88726566-88726730 | Common:6; Rare:97; Clinvar:1 | ||||
| chr16:88811895-88811970 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr16:88856882-88857153 | Common:4; Rare:127; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89102139-89102407 | Common:2; Rare:79 | ||||
| chr16:89217614-89217743 | Common:1; Rare:61 | ||||
| chr16:89508285-89508583 | Common:2; Rare:148; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:89560506-89560725 | Rare:102 | ||||
| chr16:89637820-89638236 | Common:4; Rare:164 | ||||
| chr16:89649468-89649607 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |