| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3449279-3449337 | Common:4; Rare:18 | ||||
| chr18:3449523-3449730 | Common:2; Rare:60 | ||||
| chr18:3450029-3450388 | Common:1; Rare:99 | ||||
| chr18:3451466-3451687 | Common:2; Rare:83 | ||||
| chr18:5543995-5544206 | Common:1; Rare:55 | ||||
| chr18:6414844-6415196 | Rare:105 | ||||
| chr18:8707354-8707461 | Rare:28 | ||||
| chr18:9102504-9102766 | Common:2; Rare:106; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136338-9136353 | Rare:3 | ||||
| chr18:9136522-9136880 | Rare:136 | ||||
| chr18:9136910-9137094 | Common:1; Rare:64 | ||||
| chr18:9137220-9137559 | Common:3; Rare:116 | ||||
| chr18:9334482-9334913 | Common:1; Rare:104 | ||||
| chr18:9474819-9475070 | Common:1; Rare:61 | ||||
| chr18:9615186-9615519 | Common:1; Rare:54 |