| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30748169-30748441 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761454-30761564 | Rare:41 | ||||
| chr16:30762060-30762325 | Common:3; Rare:91 | ||||
| chr16:30893941-30894275 | Common:5; Rare:91 | ||||
| chr16:30923256-30923585 | Common:1; Rare:79 | ||||
| chr16:31033298-31033576 | Common:1; Rare:90 | ||||
| chr16:31073750-31073848 | Rare:26 | ||||
| chr16:31074187-31074450 | Common:1; Rare:73 | ||||
| chr16:31108301-31108465 | Rare:41 | ||||
| chr16:31472109-31472186 | Rare:21 | ||||
| chr16:31508389-31508478 | Common:1; Rare:34 | ||||
| chr16:46689137-46689417 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689518-46689708 | Common:2; Rare:79; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973585-46973747 | Rare:73 | ||||
| chr16:47461043-47461374 | Common:2; Rare:125; Clinvar (benign):2 |