| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:649681-649837 | Rare:55 | ||||
| chr16:667940-668239 | Common:1; Rare:112 | ||||
| chr16:679982-680191 | Common:2; Rare:58 | ||||
| chr16:680254-680563 | Common:2; Rare:100 | ||||
| chr16:680660-680732 | Rare:20 | ||||
| chr16:681198-681458 | Rare:87; Clinvar (pathogenic):2 | ||||
| chr16:684123-684699 | Common:3; Rare:271 | ||||
| chr16:690305-690530 | Common:3; Rare:98 | ||||
| chr16:695285-695514 | Common:3; Rare:81 | ||||
| chr16:695690-695699 | Rare:1 | ||||
| chr16:695802-696034 | Common:2; Rare:57 | ||||
| chr16:705511-705580 | Rare:11 | ||||
| chr16:705792-706153 | Rare:94 | ||||
| chr16:714937-715204 | Common:3; Rare:100 | ||||
| chr16:715702-716009 | Common:2; Rare:92 |