| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4814613-4814912 | Common:1; Rare:79 | ||||
| chr16:4847335-4847634 | Common:2; Rare:132 | ||||
| chr16:4891850-4892085 | Common:2; Rare:111 | ||||
| chr16:5033933-5033965 | Rare:9 | ||||
| chr16:5097737-5098007 | Common:4; Rare:98 | ||||
| chr16:8797624-8797895 | Rare:107; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:10385840-10386071 | Rare:79 | ||||
| chr16:10944333-10944638 | Common:1; Rare:95 | ||||
| chr16:11668184-11668517 | Common:3; Rare:139 | ||||
| chr16:11797134-11797483 | Common:2; Rare:128 | ||||
| chr16:11851482-11851660 | Common:1; Rare:94 | ||||
| chr16:11915391-11915604 | Common:5; Rare:83 | ||||
| chr16:11976648-11976782 | Rare:53 | ||||
| chr16:14186477-14186745 | Rare:45 | ||||
| chr16:14630195-14630383 | Rare:88 |