| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11281122-11281477 | Common:3; Rare:121 | ||||
| chr16:11586891-11587018 | Common:1; Rare:39 | ||||
| chr16:11742830-11743021 | Common:2; Rare:73 | ||||
| chr16:11797176-11797499 | Common:2; Rare:124 | ||||
| chr16:11851406-11851635 | Common:1; Rare:118 | ||||
| chr16:11915150-11915371 | Common:4; Rare:68 | ||||
| chr16:11915391-11915703 | Common:5; Rare:112 | ||||
| chr16:11915854-11916250 | Common:2; Rare:158 | ||||
| chr16:11941636-11941782 | Common:3; Rare:47 | ||||
| chr16:11965239-11965443 | Rare:57 | ||||
| chr16:11976604-11976788 | Common:3; Rare:78 | ||||
| chr16:12803538-12803665 | Common:1; Rare:41 | ||||
| chr16:12803773-12803986 | Common:4; Rare:61 | ||||
| chr16:13919908-13920207 | Common:3; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:14070995-14071088 | Common:2; Rare:32 |