| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84116769-84117072 | Common:4; Rare:122 | ||||
| chr16:84699707-84700053 | Common:2; Rare:139 | ||||
| chr16:84819806-84819985 | Common:3; Rare:67 | ||||
| chr16:85027578-85027813 | Common:2; Rare:130 | ||||
| chr16:85611051-85611409 | Common:1; Rare:112 | ||||
| chr16:85613051-85613221 | Common:1; Rare:66 | ||||
| chr16:85688894-85689254 | Common:9; Rare:145 | ||||
| chr16:85799276-85799760 | Common:3; Rare:153 | ||||
| chr16:86555164-86555264 | Rare:52 | ||||
| chr16:87765908-87766044 | Rare:52 | ||||
| chr16:88570155-88570482 | Common:2; Rare:124 | ||||
| chr16:88650986-88651113 | Common:1; Rare:47; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:88663034-88663362 | Common:7; Rare:138 | ||||
| chr16:88686403-88686607 | Common:4; Rare:90 | ||||
| chr16:88706213-88706542 | Common:4; Rare:146 |