| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129772-36129971 | Common:1; Rare:81 | ||||
| chr18:36187389-36187540 | Common:3; Rare:56 | ||||
| chr18:36187848-36187965 | Rare:31 | ||||
| chr18:36297558-36297764 | Common:3; Rare:83 | ||||
| chr18:36828709-36829286 | Common:3; Rare:221 | ||||
| chr18:37565998-37566278 | Common:6; Rare:71 | ||||
| chr18:45967199-45967522 | Common:1; Rare:122; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr18:46098170-46098595 | Common:11; Rare:133; Clinvar (benign):8 | ||||
| chr18:46104184-46104439 | Common:3; Rare:79 | ||||
| chr18:46173370-46173648 | Common:1; Rare:66 | ||||
| chr18:46173938-46174164 | Common:1; Rare:57 | ||||
| chr18:46333817-46334094 | Common:1; Rare:69 | ||||
| chr18:46756810-46756939 | Common:2; Rare:37 | ||||
| chr18:46757039-46757129 | Common:3; Rare:24 | ||||
| chr18:46917331-46917628 | Common:2; Rare:123 |