| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18801497-18801830 | Common:4; Rare:115 | ||||
| chr16:19067406-19067685 | Common:5; Rare:104; Clinvar:1 | ||||
| chr16:19067796-19067932 | Common:2; Rare:33 | ||||
| chr16:19521995-19522195 | Rare:50 | ||||
| chr16:20806349-20806617 | Rare:92 | ||||
| chr16:20900843-20900895 | Rare:10 | ||||
| chr16:21599364-21599666 | Common:4; Rare:107 | ||||
| chr16:21599705-21599844 | Rare:46 | ||||
| chr16:21599847-21599885 | Rare:14 | ||||
| chr16:21953016-21953421 | Common:1; Rare:100; Clinvar (benign):3 | ||||
| chr16:22205997-22206332 | Common:1; Rare:89 | ||||
| chr16:22436912-22437013 | Rare:34 | ||||
| chr16:23453123-23453211 | Rare:29 | ||||
| chr16:23510442-23510819 | Common:4; Rare:128 | ||||
| chr16:23557207-23557559 | Common:2; Rare:135; Clinvar:1; Clinvar (benign):4 |