| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23557615-23557854 | Common:1; Rare:96 | ||||
| chr16:23557977-23558057 | Rare:30 | ||||
| chr16:23558168-23558276 | Rare:34 | ||||
| chr16:23558511-23558697 | Common:1; Rare:52 | ||||
| chr16:23595901-23595939 | Rare:8 | ||||
| chr16:23596211-23596454 | Rare:67 | ||||
| chr16:23640139-23640453 | Common:1; Rare:64 | ||||
| chr16:23640715-23640798 | Rare:18 | ||||
| chr16:23640951-23641074 | Rare:22 | ||||
| chr16:23641144-23641635 | Common:3; Rare:165; Clinvar:5; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr16:23641987-23642017 | Rare:10 | ||||
| chr16:23678624-23678953 | Common:5; Rare:100 | ||||
| chr16:23679484-23679776 | Rare:60 | ||||
| chr16:24539319-24539793 | Common:3; Rare:155 | ||||
| chr16:24539809-24539925 | Rare:24 |