| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30075840-30076357 | Common:5; Rare:336 | ||||
| chr16:30091820-30092240 | Common:4; Rare:196; Clinvar (pathogenic):1 | ||||
| chr16:30096109-30096514 | Common:3; Rare:303 | ||||
| chr16:30113423-30114644 | Common:9; Rare:331 | ||||
| chr16:30122780-30123487 | Common:23; Rare:446 | ||||
| chr16:30182735-30182870 | Rare:20 | ||||
| chr16:30182907-30183024 | Common:3; Rare:31 | ||||
| chr16:30183322-30183653 | Common:6; Rare:165 | ||||
| chr16:30354441-30355020 | Common:9; Rare:482 | ||||
| chr16:30355146-30355584 | Common:6; Rare:334 | ||||
| chr16:30355754-30355976 | Common:3; Rare:110 | ||||
| chr16:30370194-30371379 | Common:7; Rare:484 | ||||
| chr16:30377023-30377610 | Common:4; Rare:126 | ||||
| chr16:30377630-30378715 | Rare:663; Clinvar:3 | ||||
| chr16:30378670-30379090 | Common:4; Rare:181 |