| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:72093462-72093982 | Common:1; Rare:132 | ||||
| chr16:72094045-72094149 | Rare:16 | ||||
| chr16:73047819-73048066 | Rare:60 | ||||
| chr16:73048203-73048310 | Rare:18 | ||||
| chr16:73048313-73048376 | Rare:22 | ||||
| chr16:73058821-73058885 | Rare:20 | ||||
| chr16:74296450-74296891 | Common:1; Rare:140 | ||||
| chr16:74606565-74606724 | Rare:60 | ||||
| chr16:74606978-74607307 | Rare:168 | ||||
| chr16:74666646-74666659 | Rare:6 | ||||
| chr16:74666764-74667219 | Common:8; Rare:143 | ||||
| chr16:74700166-74700445 | Common:1; Rare:63 | ||||
| chr16:74700498-74700992 | Common:3; Rare:110 | ||||
| chr16:74701117-74701343 | Common:1; Rare:48 | ||||
| chr16:74774772-74775026 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):1 |