| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87765908-87766095 | Common:1; Rare:73 | ||||
| chr16:87951337-87951495 | Rare:57 | ||||
| chr16:88570159-88570531 | Common:2; Rare:135 | ||||
| chr16:88663034-88663389 | Common:9; Rare:154 | ||||
| chr16:88706192-88706578 | Common:5; Rare:173 | ||||
| chr16:88811895-88812030 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr16:88856824-88857163 | Common:4; Rare:160; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89093789-89093943 | Common:3; Rare:70 | ||||
| chr16:89217539-89217771 | Common:1; Rare:117 | ||||
| chr16:89490713-89490986 | Common:3; Rare:84 | ||||
| chr16:89491111-89491187 | Common:1; Rare:20 | ||||
| chr16:89508262-89508468 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560526-89560763 | Rare:109 | ||||
| chr16:89657631-89658091 | Common:3; Rare:242 | ||||
| chr16:89686567-89686956 | Common:10; Rare:200 |