| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698961-30699191 | Rare:87; Clinvar (benign):1 | ||||
| chr16:30748094-30748452 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30748762-30748899 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:30761305-30761705 | Common:2; Rare:208 | ||||
| chr16:30762058-30762354 | Common:3; Rare:96 | ||||
| chr16:30786710-30787070 | Common:2; Rare:85 | ||||
| chr16:30787176-30787510 | Common:1; Rare:70 | ||||
| chr16:30893980-30894370 | Common:5; Rare:98 | ||||
| chr16:30896290-30896690 | Common:2; Rare:79 | ||||
| chr16:30897021-30897246 | Common:1; Rare:39 | ||||
| chr16:30922489-30922860 | Common:2; Rare:106 | ||||
| chr16:30923248-30923611 | Common:1; Rare:88 | ||||
| chr16:30924597-30924739 | Rare:42 | ||||
| chr16:30957178-30957341 | Common:3; Rare:38 | ||||
| chr16:30957574-30957757 | Common:1; Rare:52 |