| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3443450-3443756 | Common:3; Rare:108 | ||||
| chr16:3611532-3611815 | Common:1; Rare:124; Clinvar:2 | ||||
| chr16:3717441-3717630 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:4272720-4272998 | Common:1; Rare:69 | ||||
| chr16:4273013-4273149 | Rare:33 | ||||
| chr16:4344099-4344402 | Common:2; Rare:54 | ||||
| chr16:4344422-4344455 | Common:2; Rare:1 | ||||
| chr16:4425731-4426004 | Common:1; Rare:139 | ||||
| chr16:4476270-4476474 | Common:3; Rare:77 | ||||
| chr16:4538363-4538651 | Common:4; Rare:101 | ||||
| chr16:4538759-4538867 | Rare:46 | ||||
| chr16:4614777-4615085 | Common:1; Rare:105 | ||||
| chr16:4668404-4668457 | Common:1; Rare:25 | ||||
| chr16:4693467-4693797 | Common:4; Rare:146 | ||||
| chr16:4734128-4734522 | Common:1; Rare:132 |