| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79395778-79396001 | Rare:56 | ||||
| chr18:79396533-79396571 | Common:2; Rare:13 | ||||
| chr18:79400221-79400332 | Common:2; Rare:45 | ||||
| chr18:79679163-79679575 | Common:3; Rare:183 | ||||
| chr18:79679733-79679948 | Common:3; Rare:90 | ||||
| chr18:79681875-79682070 | Common:2; Rare:45 | ||||
| chr18:79951602-79951770 | Common:2; Rare:86 | ||||
| chr18:79964477-79964673 | Common:1; Rare:59 | ||||
| chr18:79988077-79988241 | Rare:65 | ||||
| chr18:79988276-79988753 | Common:5; Rare:156; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr18:79988839-79989115 | Common:3; Rare:51 | ||||
| chr18:80033482-80033831 | Common:3; Rare:98 | ||||
| chr18:80033862-80034057 | Common:5; Rare:32 | ||||
| chr18:80034160-80034790 | Common:6; Rare:241 | ||||
| chr18:80108776-80109093 | Common:1; Rare:76 |