| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87317320-87317560 | Common:7; Rare:98 | ||||
| chr16:87765886-87766061 | Common:1; Rare:72 | ||||
| chr16:88570155-88570541 | Common:2; Rare:141 | ||||
| chr16:88651017-88651127 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr16:88663070-88663382 | Common:9; Rare:130 | ||||
| chr16:88706203-88706555 | Common:4; Rare:156 | ||||
| chr16:88811877-88811996 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr16:88856568-88856727 | Common:5; Rare:27 | ||||
| chr16:88856810-88857188 | Common:4; Rare:184; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89088224-89088396 | Common:2; Rare:34 | ||||
| chr16:89093769-89093951 | Common:3; Rare:78 | ||||
| chr16:89200124-89200244 | Rare:35 | ||||
| chr16:89217607-89217771 | Common:1; Rare:85 | ||||
| chr16:89507991-89508087 | Rare:28 | ||||
| chr16:89508312-89508463 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |