| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:68714539-68714726 | Common:1; Rare:52 | ||||
| chr18:68714955-68715430 | Common:8; Rare:181 | ||||
| chr18:69947501-69947958 | Common:2; Rare:78 | ||||
| chr18:69956069-69956261 | Rare:37 | ||||
| chr18:69956636-69956752 | Common:1; Rare:24 | ||||
| chr18:69956857-69957013 | Common:2; Rare:23 | ||||
| chr18:70028223-70028285 | Common:1; Rare:6 | ||||
| chr18:70028820-70029015 | Common:1; Rare:43 | ||||
| chr18:70205592-70205829 | Common:3; Rare:101; Clinvar (benign):2 | ||||
| chr18:70205847-70205872 | Rare:5 | ||||
| chr18:70205969-70206219 | Rare:79 | ||||
| chr18:70288568-70288685 | Rare:31 | ||||
| chr18:70288708-70288933 | Common:2; Rare:80 | ||||
| chr18:70288939-70289108 | Common:2; Rare:49 | ||||
| chr18:70289231-70289402 | Common:2; Rare:36 |