| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3611554-3611806 | Rare:106; Clinvar:1 | ||||
| chr16:4351239-4351533 | Common:2; Rare:127 | ||||
| chr16:4371609-4371897 | Common:1; Rare:104 | ||||
| chr16:4425767-4425994 | Common:1; Rare:117 | ||||
| chr16:4476270-4476486 | Common:3; Rare:80 | ||||
| chr16:4538380-4538626 | Common:4; Rare:85 | ||||
| chr16:4538713-4538852 | Rare:56 | ||||
| chr16:4614844-4615047 | Common:1; Rare:55 | ||||
| chr16:4616179-4616504 | Rare:84 | ||||
| chr16:4734155-4734537 | Common:1; Rare:126 | ||||
| chr16:4767120-4767349 | Common:2; Rare:78 | ||||
| chr16:5033920-5033976 | Rare:23 | ||||
| chr16:5065916-5066247 | Common:1; Rare:102 | ||||
| chr16:5071775-5071909 | Rare:78; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:5097728-5097988 | Common:4; Rare:96 |