| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20806349-20806659 | Rare:100 | ||||
| chr16:21953028-21953419 | Common:1; Rare:99; Clinvar (benign):3 | ||||
| chr16:22436961-22437041 | Rare:28 | ||||
| chr16:23453147-23453215 | Rare:21 | ||||
| chr16:23557325-23557472 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641247-23641530 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678714-23678947 | Common:4; Rare:73 | ||||
| chr16:24539331-24539580 | Common:1; Rare:77 | ||||
| chr16:24729607-24729727 | Common:6; Rare:67 | ||||
| chr16:25015291-25015457 | Common:2; Rare:61 | ||||
| chr16:25111472-25111796 | Common:2; Rare:83 | ||||
| chr16:27268724-27268851 | Common:1; Rare:40 | ||||
| chr16:27313804-27313949 | Common:1; Rare:39 | ||||
| chr16:27549877-27550167 | Common:2; Rare:111 | ||||
| chr16:28822580-28822739 | Rare:59 |