| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54828326-54828618 | Rare:66 | ||||
| chr18:54959352-54959539 | Common:2; Rare:50 | ||||
| chr18:55586117-55586152 | Rare:14 | ||||
| chr18:55589715-55590033 | Common:2; Rare:107 | ||||
| chr18:56651133-56651379 | Common:3; Rare:62 | ||||
| chr18:57586567-57586748 | Rare:59 | ||||
| chr18:57621706-57622000 | Common:3; Rare:106 | ||||
| chr18:58221410-58221608 | Common:1; Rare:35 | ||||
| chr18:58628761-58629217 | Common:4; Rare:74 | ||||
| chr18:58671202-58671420 | Rare:90 | ||||
| chr18:59139689-59140035 | Common:3; Rare:92 | ||||
| chr18:59359177-59359517 | Common:4; Rare:154; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:59899849-59900063 | Common:3; Rare:68 | ||||
| chr18:62186924-62187320 | Common:5; Rare:111 | ||||
| chr18:62526762-62526892 | Common:2; Rare:63 |