| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689115-46689337 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689396-46689776 | Common:3; Rare:141; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46689863-46690015 | Rare:32 | ||||
| chr16:46690038-46690106 | Common:1; Rare:17 | ||||
| chr16:46690111-46690278 | Rare:39 | ||||
| chr16:46789875-46790345 | Common:5; Rare:105 | ||||
| chr16:46830306-46830469 | Common:1; Rare:36 | ||||
| chr16:46830643-46830728 | Common:1; Rare:22 | ||||
| chr16:46830756-46830792 | Rare:5 | ||||
| chr16:46830963-46831325 | Common:2; Rare:134 | ||||
| chr16:46831363-46831627 | Common:1; Rare:75 | ||||
| chr16:46883807-46884156 | Common:2; Rare:78 | ||||
| chr16:46884158-46884463 | Common:1; Rare:85 | ||||
| chr16:46885261-46885341 | Rare:10 | ||||
| chr16:46972500-46972698 | Common:1; Rare:53 |