| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74606914-74607290 | Rare:380 | ||||
| chr16:74666771-74667221 | Common:24; Rare:415 | ||||
| chr16:74700721-74700963 | Rare:48 | ||||
| chr16:74774611-74775085 | Common:14; Rare:358; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr16:74984979-74985358 | Common:4; Rare:211 | ||||
| chr16:74998682-74999201 | Common:11; Rare:487 | ||||
| chr16:74999213-74999695 | Common:11; Rare:333 | ||||
| chr16:74999862-75000445 | Common:6; Rare:290 | ||||
| chr16:75000467-75000867 | Common:3; Rare:128 | ||||
| chr16:75116703-75116899 | Common:4; Rare:80 | ||||
| chr16:75148490-75148596 | Common:2; Rare:48 | ||||
| chr16:75148722-75149113 | Common:8; Rare:357 | ||||
| chr16:75250148-75250762 | Common:6; Rare:181 | ||||
| chr16:75250820-75250948 | Common:1; Rare:34 | ||||
| chr16:75251609-75251906 | Common:2; Rare:261 |