| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:9913833-9914111 | Common:1; Rare:106 | ||||
| chr18:10455113-10455348 | Common:2; Rare:65 | ||||
| chr18:11851246-11851427 | Common:1; Rare:60 | ||||
| chr18:12307936-12308297 | Common:6; Rare:137 | ||||
| chr18:12702678-12703084 | Common:3; Rare:166 | ||||
| chr18:12884167-12884522 | Common:6; Rare:165 | ||||
| chr18:12947673-12948061 | Common:3; Rare:100 | ||||
| chr18:13726453-13726726 | Common:3; Rare:106 | ||||
| chr18:22933840-22933883 | Common:1; Rare:15 | ||||
| chr18:23453176-23453345 | Rare:58 | ||||
| chr18:23503316-23503537 | Common:1; Rare:77 | ||||
| chr18:23586416-23586537 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:25352086-25352410 | Common:2; Rare:131 | ||||
| chr18:32092423-32092727 | Common:4; Rare:140 | ||||
| chr18:35240879-35241088 | Common:3; Rare:79 |