| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:18926114-18926135 | Rare:8 | ||||
| chr16:19067455-19067702 | Common:5; Rare:104; Clinvar:1 | ||||
| chr16:19067805-19067941 | Common:2; Rare:33 | ||||
| chr16:19521710-19521731 | Rare:6 | ||||
| chr16:19521995-19522249 | Rare:65 | ||||
| chr16:19555455-19555733 | Common:2; Rare:124 | ||||
| chr16:19862000-19862182 | Rare:34 | ||||
| chr16:20741735-20741979 | Common:1; Rare:109 | ||||
| chr16:20806331-20806610 | Rare:92 | ||||
| chr16:20900226-20900840 | Common:4; Rare:146 | ||||
| chr16:21158547-21158712 | Common:1; Rare:49 | ||||
| chr16:21652594-21652723 | Rare:34 | ||||
| chr16:21953005-21953429 | Common:1; Rare:105; Clinvar (benign):3 | ||||
| chr16:22437110-22437313 | Rare:68 | ||||
| chr16:23453127-23453242 | Rare:32 |