| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75647580-75647873 | Common:4; Rare:146; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648153-75648448 | Rare:112 | ||||
| chr16:75648504-75648549 | Rare:12 | ||||
| chr16:77190704-77191231 | Common:12; Rare:179 | ||||
| chr16:77211972-77212129 | Common:2; Rare:39 | ||||
| chr16:77212437-77212466 | Rare:6 | ||||
| chr16:78099512-78099799 | Common:2; Rare:128; Clinvar (benign):6 | ||||
| chr16:79599783-79599855 | Rare:16 | ||||
| chr16:79600027-79600378 | Common:4; Rare:120 | ||||
| chr16:79600647-79600958 | Common:2; Rare:96 | ||||
| chr16:80540825-80541034 | Common:5; Rare:84 | ||||
| chr16:81006306-81006565 | Common:3; Rare:63 | ||||
| chr16:81006798-81007263 | Common:5; Rare:157 | ||||
| chr16:81077218-81077291 | Rare:28 | ||||
| chr16:81181307-81181477 | Rare:45 |