| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:81006833-81007284 | Common:3; Rare:150 | ||||
| chr16:84116806-84117061 | Common:3; Rare:99 | ||||
| chr16:84145123-84145292 | Common:1; Rare:84; Clinvar:1 | ||||
| chr16:84504588-84504861 | Common:8; Rare:119 | ||||
| chr16:85027618-85027813 | Common:1; Rare:103 | ||||
| chr16:85799520-85799757 | Common:2; Rare:69 | ||||
| chr16:86555182-86555279 | Rare:51 | ||||
| chr16:87317331-87317516 | Common:6; Rare:71 | ||||
| chr16:87765919-87766033 | Rare:45 | ||||
| chr16:88570174-88570461 | Common:1; Rare:109 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88856913-88857148 | Common:4; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217619-89217728 | Common:1; Rare:50 | ||||
| chr16:89508318-89508424 | Rare:59; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560526-89560717 | Rare:82 |