| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88881120-88881322 | Common:2; Rare:89 | ||||
| chr16:89217612-89217776 | Common:1; Rare:84 | ||||
| chr16:89508318-89508583 | Common:2; Rare:129; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:89560560-89560717 | Rare:65 | ||||
| chr16:89657631-89658095 | Common:3; Rare:243 | ||||
| chr16:89686661-89686713 | Common:4; Rare:36 | ||||
| chr16:89686907-89686967 | Rare:24 | ||||
| chr16:89701666-89701782 | Rare:49 | ||||
| chr16:89720857-89721041 | Common:1; Rare:58 | ||||
| chr16:89722850-89723159 | Common:3; Rare:129 | ||||
| chr16:89816640-89816772 | Common:2; Rare:58; Clinvar:2 | ||||
| chr16:89873482-89873856 | Common:3; Rare:168 | ||||
| chr16:89972478-89972651 | Common:1; Rare:66 | ||||
| chr17:714696-714953 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr17:732261-732732 | Common:3; Rare:164 |