| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46088824-46089167 | Common:1; Rare:92 | ||||
| chr18:46097813-46098056 | Common:2; Rare:74 | ||||
| chr18:46098233-46098377 | Common:11; Rare:63; Clinvar (benign):6 | ||||
| chr18:46098562-46098614 | Rare:13 | ||||
| chr18:46104137-46104444 | Common:4; Rare:94; Clinvar (benign):1 | ||||
| chr18:46104631-46104779 | Common:2; Rare:32 | ||||
| chr18:46104784-46104801 | Rare:3 | ||||
| chr18:46104841-46104972 | Rare:26 | ||||
| chr18:46173486-46173649 | Rare:41 | ||||
| chr18:46173878-46174162 | Common:1; Rare:67 | ||||
| chr18:46917384-46917645 | Common:3; Rare:112 | ||||
| chr18:47150114-47150236 | Common:1; Rare:40 | ||||
| chr18:47150394-47150630 | Common:4; Rare:102 | ||||
| chr18:47176280-47176479 | Common:1; Rare:83; Clinvar (benign):1 | ||||
| chr18:47930170-47930330 | Rare:61 |