| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89508011-89508096 | Rare:27 | ||||
| chr16:89508192-89508467 | Common:2; Rare:145; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89508809-89509061 | Rare:107 | ||||
| chr16:89560356-89560819 | Common:1; Rare:198 | ||||
| chr16:89561187-89561453 | Common:1; Rare:111 | ||||
| chr16:89574976-89575401 | Common:2; Rare:105 | ||||
| chr16:89575720-89575839 | Common:1; Rare:40 | ||||
| chr16:89616600-89616721 | Common:1; Rare:36 | ||||
| chr16:89657573-89658138 | Common:4; Rare:281; Clinvar (benign):1 | ||||
| chr16:89686522-89686813 | Common:10; Rare:144 | ||||
| chr16:89686844-89687082 | Common:3; Rare:95 | ||||
| chr16:89701546-89701733 | Common:2; Rare:61 | ||||
| chr16:89701969-89702243 | Common:8; Rare:84 | ||||
| chr16:89711663-89712004 | Common:3; Rare:133 | ||||
| chr16:89712065-89712094 | Rare:12 |