| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55588114-55588179 | Rare:18; Clinvar (benign):1 | ||||
| chr18:55589715-55589908 | Rare:54 | ||||
| chr18:56651129-56651432 | Common:4; Rare:80 | ||||
| chr18:57586601-57586813 | Rare:60 | ||||
| chr18:57621713-57621964 | Common:3; Rare:90 | ||||
| chr18:58628751-58629444 | Common:4; Rare:122 | ||||
| chr18:58864742-58864902 | Rare:33 | ||||
| chr18:59139714-59139996 | Common:2; Rare:76 | ||||
| chr18:59899884-59899997 | Common:2; Rare:33 | ||||
| chr18:60372773-60372932 | Rare:29 | ||||
| chr18:62186915-62187329 | Common:5; Rare:116 | ||||
| chr18:63367138-63367386 | Common:1; Rare:88 | ||||
| chr18:63422370-63422677 | Common:2; Rare:85 | ||||
| chr18:68714977-68715379 | Common:7; Rare:158 | ||||
| chr18:70205648-70205833 | Common:3; Rare:77; Clinvar (benign):2 |