| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71809076-71809338 | Common:3; Rare:82 | ||||
| chr16:71845895-71846013 | Common:2; Rare:38 | ||||
| chr16:71895250-71895574 | Common:2; Rare:126 | ||||
| chr16:72093494-72093934 | Rare:111 | ||||
| chr16:74296661-74296882 | Rare:83 | ||||
| chr16:74607080-74607200 | Rare:61 | ||||
| chr16:74666830-74667177 | Common:7; Rare:117 | ||||
| chr16:74701140-74701343 | Common:1; Rare:47 | ||||
| chr16:75148369-75148551 | Common:4; Rare:76 | ||||
| chr16:75433416-75433852 | Common:4; Rare:135 | ||||
| chr16:75464380-75464454 | Common:2; Rare:29 | ||||
| chr16:75566242-75566431 | Common:1; Rare:97 | ||||
| chr16:75623229-75623390 | Common:3; Rare:55 | ||||
| chr16:75647614-75647788 | Common:1; Rare:89; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648636-75648658 | Rare:12 |