| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85027572-85027792 | Common:2; Rare:122 | ||||
| chr16:85613038-85613328 | Common:1; Rare:109 | ||||
| chr16:85688878-85689243 | Common:10; Rare:149 | ||||
| chr16:85799321-85799752 | Common:3; Rare:133 | ||||
| chr16:85898994-85899185 | Common:3; Rare:53 | ||||
| chr16:85908553-85908702 | Common:1; Rare:28 | ||||
| chr16:86555174-86555332 | Rare:84 | ||||
| chr16:87317394-87317527 | Common:2; Rare:51 | ||||
| chr16:87701087-87701345 | Common:1; Rare:81 | ||||
| chr16:87701638-87701881 | Common:1; Rare:103 | ||||
| chr16:87765886-87766061 | Common:1; Rare:72 | ||||
| chr16:87951349-87951506 | Rare:59 | ||||
| chr16:88570174-88570416 | Common:1; Rare:87 | ||||
| chr16:88650995-88651174 | Common:1; Rare:53; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:88663037-88663382 | Common:9; Rare:147 |