| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1308866-1309152 | Common:3; Rare:75 | ||||
| chr16:1309381-1309696 | Rare:114 | ||||
| chr16:1333481-1333656 | Common:2; Rare:73 | ||||
| chr16:1335981-1336381 | Common:4; Rare:152 | ||||
| chr16:1351750-1352070 | Common:2; Rare:147; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1379570-1379920 | Common:4; Rare:128 | ||||
| chr16:1420684-1421041 | Common:1; Rare:144 | ||||
| chr16:1474860-1475300 | Common:6; Rare:152; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:1493219-1493587 | Common:4; Rare:109 | ||||
| chr16:1609998-1610103 | Rare:28 | ||||
| chr16:1610290-1610447 | Rare:38 | ||||
| chr16:1610560-1610890 | Common:1; Rare:105; Clinvar:1 | ||||
| chr16:1611985-1612415 | Common:2; Rare:156; Clinvar:2 | ||||
| chr16:1614414-1614934 | Common:2; Rare:169 | ||||
| chr16:1677997-1678315 | Common:3; Rare:105 |