| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84504612-84504853 | Common:8; Rare:105 | ||||
| chr16:85027603-85027809 | Common:1; Rare:111 | ||||
| chr16:85799526-85799748 | Common:2; Rare:64 | ||||
| chr16:85898998-85899179 | Common:3; Rare:50 | ||||
| chr16:86555172-86555327 | Rare:80 | ||||
| chr16:87317393-87317539 | Common:3; Rare:54 | ||||
| chr16:87383707-87383960 | Common:1; Rare:102 | ||||
| chr16:87765901-87766055 | Common:1; Rare:63 | ||||
| chr16:88570174-88570467 | Common:1; Rare:111 | ||||
| chr16:88663078-88663374 | Common:8; Rare:121 | ||||
| chr16:88706338-88706527 | Common:3; Rare:93 | ||||
| chr16:88719802-88720099 | Common:4; Rare:132 | ||||
| chr16:88856932-88857183 | Common:4; Rare:117; Clinvar (benign):2 | ||||
| chr16:89217619-89217738 | Common:1; Rare:56 | ||||
| chr16:89508296-89508424 | Rare:72; Clinvar:1; Clinvar (pathogenic):1 |