| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3611564-3611826 | Common:1; Rare:111; Clinvar:1 | ||||
| chr16:3717499-3717635 | Rare:71; Clinvar:1 | ||||
| chr16:3781083-3781248 | Common:3; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:4344047-4344812 | Common:14; Rare:105 | ||||
| chr16:4425745-4425892 | Common:1; Rare:70 | ||||
| chr16:4476317-4476483 | Rare:65 | ||||
| chr16:4538394-4538636 | Common:3; Rare:82 | ||||
| chr16:4611016-4611162 | Common:1; Rare:27 | ||||
| chr16:4614783-4615046 | Common:1; Rare:88 | ||||
| chr16:4668458-4668525 | Common:3; Rare:37 | ||||
| chr16:4693664-4693786 | Common:2; Rare:71 | ||||
| chr16:4698936-4699095 | Common:1; Rare:80 | ||||
| chr16:4734151-4734542 | Common:1; Rare:127 | ||||
| chr16:4814409-4814635 | Common:1; Rare:80 | ||||
| chr16:4846173-4846327 | Common:1; Rare:44 |