| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22933141-22933484 | Common:5; Rare:111; Clinvar:5; Clinvar (benign):3 | ||||
| chr18:22933595-22933922 | Common:2; Rare:112 | ||||
| chr18:23134366-23134599 | Common:3; Rare:42 | ||||
| chr18:23135309-23135769 | Common:5; Rare:121 | ||||
| chr18:23135945-23136050 | Rare:30 | ||||
| chr18:23136202-23136276 | Rare:17 | ||||
| chr18:23136510-23136610 | Rare:26 | ||||
| chr18:23136657-23136885 | Common:3; Rare:57 | ||||
| chr18:23437674-23437685 | Rare:2 | ||||
| chr18:23437888-23437989 | Common:2; Rare:60 | ||||
| chr18:23452802-23452893 | Common:1; Rare:18 | ||||
| chr18:23453029-23453440 | Rare:127 | ||||
| chr18:23453506-23453546 | Rare:16 | ||||
| chr18:23453770-23453959 | Common:1; Rare:31 | ||||
| chr18:23503085-23503145 | Rare:14 |