| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11851517-11851635 | Rare:57 | ||||
| chr16:11915883-11916020 | Common:2; Rare:84 | ||||
| chr16:11976615-11976760 | Common:2; Rare:53 | ||||
| chr16:14071269-14071345 | Rare:25 | ||||
| chr16:14630188-14630430 | Rare:105 | ||||
| chr16:14632713-14632981 | Common:1; Rare:94 | ||||
| chr16:15094241-15094409 | Rare:81 | ||||
| chr16:18790256-18790484 | Common:4; Rare:81 | ||||
| chr16:18801462-18801831 | Common:4; Rare:131 | ||||
| chr16:18926391-18926627 | Common:2; Rare:96 | ||||
| chr16:19067455-19067617 | Common:4; Rare:43 | ||||
| chr16:20741787-20741996 | Common:1; Rare:88 | ||||
| chr16:20806367-20806533 | Rare:64 | ||||
| chr16:21953003-21953391 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr16:22436949-22437071 | Rare:46 |