| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:48860012-48860059 | Rare:12 | ||||
| chr18:48860355-48860515 | Common:1; Rare:40 | ||||
| chr18:49460550-49460837 | Common:2; Rare:89; Clinvar:6; Clinvar (benign):1 | ||||
| chr18:49486396-49486698 | Common:2; Rare:58 | ||||
| chr18:49486962-49487071 | Rare:37 | ||||
| chr18:49487092-49487431 | Common:4; Rare:133 | ||||
| chr18:49491345-49491637 | Common:1; Rare:97 | ||||
| chr18:49491727-49491980 | Common:1; Rare:81 | ||||
| chr18:49492369-49492588 | Common:1; Rare:91 | ||||
| chr18:49561852-49562099 | Rare:69 | ||||
| chr18:49812874-49813069 | Common:1; Rare:38 | ||||
| chr18:49813461-49813574 | Rare:31 | ||||
| chr18:49813829-49814066 | Common:1; Rare:104 | ||||
| chr18:49814379-49814456 | Rare:25 | ||||
| chr18:50266442-50266604 | Common:1; Rare:64 |