| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23557629-23557736 | Rare:38 | ||||
| chr16:23561059-23561211 | Rare:34 | ||||
| chr16:23596205-23596410 | Rare:63 | ||||
| chr16:23641212-23641545 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678735-23679238 | Common:4; Rare:152 | ||||
| chr16:24539343-24539654 | Common:1; Rare:114 | ||||
| chr16:24729597-24729846 | Common:7; Rare:105 | ||||
| chr16:25015296-25015515 | Common:2; Rare:73 | ||||
| chr16:25111472-25111893 | Common:2; Rare:129 | ||||
| chr16:25257807-25258045 | Common:6; Rare:104 | ||||
| chr16:25258288-25258385 | Common:4; Rare:53 | ||||
| chr16:27203411-27203540 | Rare:38 | ||||
| chr16:27233095-27233253 | Common:1; Rare:35 | ||||
| chr16:27268704-27268877 | Common:1; Rare:66 | ||||
| chr16:27313702-27313959 | Common:5; Rare:68 |