| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75433339-75433812 | Common:4; Rare:153 | ||||
| chr16:75464380-75464448 | Common:2; Rare:28 | ||||
| chr16:75566831-75566865 | Rare:10 | ||||
| chr16:75647605-75647837 | Common:2; Rare:114; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648636-75648658 | Rare:12 | ||||
| chr16:77191144-77191239 | Common:1; Rare:41 | ||||
| chr16:79600732-79600953 | Common:1; Rare:63 | ||||
| chr16:81006430-81006581 | Rare:47 | ||||
| chr16:81006798-81007263 | Common:5; Rare:157 | ||||
| chr16:82626866-82627097 | Rare:69 | ||||
| chr16:84116739-84117066 | Common:4; Rare:133 | ||||
| chr16:85027620-85027813 | Common:1; Rare:102 | ||||
| chr16:85799321-85799776 | Common:3; Rare:141 | ||||
| chr16:87765919-87766028 | Rare:44 | ||||
| chr16:88570208-88570489 | Common:1; Rare:116 |