| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22206034-22206359 | Common:1; Rare:90 | ||||
| chr16:22436954-22437326 | Rare:130 | ||||
| chr16:22437476-22437676 | Common:2; Rare:48 | ||||
| chr16:23452688-23452799 | Rare:39 | ||||
| chr16:23453127-23453231 | Rare:31 | ||||
| chr16:23557318-23557551 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641223-23641545 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678714-23678947 | Common:4; Rare:73 | ||||
| chr16:23837180-23837406 | Rare:40 | ||||
| chr16:24185235-24185565 | Rare:65 | ||||
| chr16:24539431-24539630 | Common:1; Rare:78 | ||||
| chr16:24729604-24729745 | Common:6; Rare:74 | ||||
| chr16:25015223-25015462 | Common:2; Rare:74 | ||||
| chr16:25111478-25111814 | Common:2; Rare:93 | ||||
| chr16:27268717-27268877 | Common:1; Rare:57 |