| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71845895-71846023 | Common:2; Rare:41 | ||||
| chr16:71894416-71894447 | Rare:10 | ||||
| chr16:71895254-71895584 | Common:3; Rare:126 | ||||
| chr16:72008532-72008778 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr16:72093511-72093957 | Rare:115 | ||||
| chr16:74296456-74296988 | Common:1; Rare:176 | ||||
| chr16:74607042-74607213 | Rare:95 | ||||
| chr16:74666784-74667098 | Common:5; Rare:117 | ||||
| chr16:74700541-74700673 | Rare:31 | ||||
| chr16:74700677-74700711 | Rare:5 | ||||
| chr16:74700748-74700985 | Common:2; Rare:49 | ||||
| chr16:74701041-74701386 | Common:4; Rare:66 | ||||
| chr16:74985035-74985372 | Common:2; Rare:108 | ||||
| chr16:75148945-75149063 | Common:1; Rare:50 | ||||
| chr16:75433348-75433812 | Common:4; Rare:150 |