| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4425767-4425879 | Common:1; Rare:52 | ||||
| chr16:4476284-4476452 | Common:2; Rare:64 | ||||
| chr16:4538409-4538619 | Common:2; Rare:73 | ||||
| chr16:4693489-4693723 | Common:2; Rare:101 | ||||
| chr16:4734199-4734540 | Common:1; Rare:110 | ||||
| chr16:4767134-4767360 | Common:1; Rare:76 | ||||
| chr16:5097746-5098015 | Common:4; Rare:91 | ||||
| chr16:8797647-8797866 | Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:10580569-10580781 | Rare:67 | ||||
| chr16:10743744-10743855 | Rare:39 | ||||
| chr16:11587171-11587302 | Common:1; Rare:29 | ||||
| chr16:11851517-11851635 | Rare:57 | ||||
| chr16:11976648-11976772 | Rare:47 | ||||
| chr16:14071024-14071355 | Common:3; Rare:112 | ||||
| chr16:14632713-14632981 | Common:1; Rare:94 |