| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31180564-31180871 | Common:3; Rare:109 | ||||
| chr16:31442766-31443059 | Common:1; Rare:47 | ||||
| chr16:31459091-31459161 | Rare:23 | ||||
| chr16:31459267-31459517 | Common:1; Rare:104 | ||||
| chr16:31471901-31472181 | Rare:61 | ||||
| chr16:31508363-31508516 | Common:4; Rare:65 | ||||
| chr16:31713123-31713367 | Common:1; Rare:59 | ||||
| chr16:31873633-31873955 | Common:1; Rare:102 | ||||
| chr16:32254025-32254231 | Common:2; Rare:29 | ||||
| chr16:46621316-46621496 | Rare:72 | ||||
| chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689500-46689768 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46789922-46790101 | Common:5; Rare:42 | ||||
| chr16:46831111-46831325 | Common:2; Rare:84 | ||||
| chr16:46973532-46973827 | Rare:122 |