| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22436942-22437067 | Rare:46 | ||||
| chr16:22437137-22437341 | Rare:65 | ||||
| chr16:22437446-22437490 | Rare:12 | ||||
| chr16:22437505-22437682 | Common:2; Rare:45 | ||||
| chr16:23452688-23452808 | Rare:44 | ||||
| chr16:23452965-23453102 | Rare:36 | ||||
| chr16:23557313-23557530 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641247-23641530 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24729604-24729739 | Common:6; Rare:71 | ||||
| chr16:25015244-25015457 | Common:2; Rare:69 | ||||
| chr16:25111521-25111805 | Common:2; Rare:83 | ||||
| chr16:27268724-27268851 | Common:1; Rare:40 | ||||
| chr16:27313478-27313601 | Common:2; Rare:30 | ||||
| chr16:27313767-27313993 | Common:5; Rare:64 | ||||
| chr16:27314409-27314668 | Common:1; Rare:52 |