| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3443461-3443745 | Common:3; Rare:99 | ||||
| chr16:3457946-3458111 | Common:2; Rare:79 | ||||
| chr16:3611578-3611804 | Rare:97 | ||||
| chr16:4371688-4371882 | Rare:73 | ||||
| chr16:4425752-4425911 | Common:1; Rare:84 | ||||
| chr16:4476286-4476467 | Common:2; Rare:70 | ||||
| chr16:4538427-4538621 | Common:2; Rare:72 | ||||
| chr16:4693476-4693741 | Common:3; Rare:118 | ||||
| chr16:4734157-4734520 | Common:1; Rare:119 | ||||
| chr16:4847226-4847493 | Common:2; Rare:124 | ||||
| chr16:5071784-5071852 | Rare:32; Clinvar (benign):1 | ||||
| chr16:8797631-8797885 | Rare:100; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868977-8869272 | Common:4; Rare:131 | ||||
| chr16:10743796-10743884 | Rare:36 | ||||
| chr16:10944327-10944638 | Common:1; Rare:97 |