| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:101652334-101652519 | Common:3; Rare:87 | ||||
| chr16:53590-53902 | Common:7; Rare:106 | ||||
| chr16:78084-78282 | Common:3; Rare:72 | ||||
| chr16:684330-684460 | Common:2; Rare:68 | ||||
| chr16:740986-741102 | Rare:38 | ||||
| chr16:1308895-1309199 | Common:2; Rare:79 | ||||
| chr16:1706076-1706281 | Common:1; Rare:57 | ||||
| chr16:1771521-1771853 | Common:3; Rare:128 | ||||
| chr16:1782632-1783010 | Common:1; Rare:123 | ||||
| chr16:1943189-1943500 | Common:1; Rare:93 | ||||
| chr16:1964566-1964944 | Common:14; Rare:166 | ||||
| chr16:1971920-1972123 | Common:1; Rare:59 | ||||
| chr16:2047804-2048033 | Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268069-2268186 | Common:1; Rare:56 | ||||
| chr16:2459980-2460123 | Rare:37 |