| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71230664-71230805 | Rare:43 | ||||
| chr16:71289353-71289459 | Rare:34 | ||||
| chr16:71358605-71358886 | Common:1; Rare:100 | ||||
| chr16:71564911-71565021 | Common:1; Rare:38 | ||||
| chr16:71808774-71808885 | Common:1; Rare:60 | ||||
| chr16:71809042-71809344 | Common:3; Rare:97 | ||||
| chr16:71845906-71846017 | Common:1; Rare:34 | ||||
| chr16:71883913-71884279 | Common:1; Rare:110 | ||||
| chr16:71884613-71884678 | Rare:10 | ||||
| chr16:71895337-71895584 | Common:1; Rare:84 | ||||
| chr16:72008573-72008760 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr16:72093598-72093993 | Common:1; Rare:94 | ||||
| chr16:74296439-74296941 | Common:1; Rare:168 | ||||
| chr16:74607061-74607206 | Rare:79 | ||||
| chr16:74666891-74667082 | Common:1; Rare:66 |