| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15856939-15857175 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:15888560-15888803 | Common:2; Rare:93 | ||||
| chr16:18801449-18801830 | Common:4; Rare:133 | ||||
| chr16:18925738-18925923 | Common:2; Rare:63 | ||||
| chr16:18926114-18926204 | Common:2; Rare:41 | ||||
| chr16:18926387-18926699 | Common:2; Rare:113 | ||||
| chr16:19067445-19067696 | Common:5; Rare:103; Clinvar:1 | ||||
| chr16:19067814-19067932 | Common:2; Rare:30 | ||||
| chr16:19113758-19113968 | Common:1; Rare:43 | ||||
| chr16:19555655-19555732 | Common:2; Rare:41 | ||||
| chr16:19691156-19691307 | Common:1; Rare:30 | ||||
| chr16:20763942-20764029 | Common:1; Rare:14 | ||||
| chr16:20806337-20806687 | Rare:107 | ||||
| chr16:20900226-20900873 | Common:4; Rare:154 | ||||
| chr16:21158524-21158740 | Common:1; Rare:63 |