| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57544260-57544571 | Rare:59 | ||||
| chr16:57591110-57591430 | Common:4; Rare:76 | ||||
| chr16:57601670-57602530 | Common:9; Rare:224 | ||||
| chr16:57609540-57610120 | Common:6; Rare:186 | ||||
| chr16:57611319-57611440 | Rare:23 | ||||
| chr16:57689820-57690160 | Common:2; Rare:307 | ||||
| chr16:57734945-57735076 | Common:3; Rare:32 | ||||
| chr16:57810280-57810570 | Common:3; Rare:154 | ||||
| chr16:57816430-57816567 | Rare:67 | ||||
| chr16:57900310-57900560 | Rare:44 | ||||
| chr16:58002528-58003041 | Rare:186; Clinvar (pathogenic):4 | ||||
| chr16:58016130-58016510 | Rare:65 | ||||
| chr16:58103144-58103544 | Common:4; Rare:86 | ||||
| chr16:58215020-58215310 | Common:3; Rare:52 | ||||
| chr16:58243430-58244602 | Common:6; Rare:278 |