| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89560317-89560400 | Rare:25 | ||||
| chr16:89560402-89560753 | Common:1; Rare:162 | ||||
| chr16:89561039-89561069 | Common:1; Rare:8 | ||||
| chr16:89561156-89561430 | Common:1; Rare:109 | ||||
| chr16:89575654-89575847 | Common:2; Rare:71 | ||||
| chr16:89575960-89576052 | Common:1; Rare:14 | ||||
| chr16:89657587-89658145 | Common:5; Rare:275; Clinvar (benign):1 | ||||
| chr16:89686526-89686801 | Common:9; Rare:137 | ||||
| chr16:89686822-89687069 | Common:4; Rare:110 | ||||
| chr16:89687244-89687521 | Rare:78 | ||||
| chr16:89701175-89701221 | Rare:13 | ||||
| chr16:89701524-89701831 | Common:2; Rare:104 | ||||
| chr16:89701953-89702270 | Common:9; Rare:99 | ||||
| chr16:89711960-89712108 | Rare:57 | ||||
| chr16:89712484-89712731 | Common:3; Rare:114 |