| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:275862-276037 | Common:5; Rare:47 | ||||
| chr16:401715-401955 | Common:2; Rare:101 | ||||
| chr16:636270-636456 | Common:4; Rare:56 | ||||
| chr16:649004-649395 | Common:3; Rare:111 | ||||
| chr16:684330-684450 | Common:1; Rare:63 | ||||
| chr16:740986-741131 | Rare:47 | ||||
| chr16:970845-971139 | Common:7; Rare:138 | ||||
| chr16:980803-981102 | Common:4; Rare:79 | ||||
| chr16:1420714-1420975 | Common:1; Rare:107 | ||||
| chr16:1533487-1533694 | Common:1; Rare:40 | ||||
| chr16:1612032-1612366 | Common:2; Rare:114; Clinvar:1 | ||||
| chr16:1706086-1706469 | Common:4; Rare:117; Clinvar (pathogenic):1 | ||||
| chr16:1771521-1771848 | Common:3; Rare:127 | ||||
| chr16:1773115-1773215 | Rare:28 | ||||
| chr16:1826772-1827019 | Common:5; Rare:86 |