| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:62186937-62187340 | Common:5; Rare:110 | ||||
| chr18:63367089-63367328 | Common:1; Rare:84 | ||||
| chr18:63422344-63422716 | Common:2; Rare:111 | ||||
| chr18:63476847-63476997 | Rare:35 | ||||
| chr18:63970000-63970174 | Common:4; Rare:39 | ||||
| chr18:68714977-68715260 | Common:5; Rare:126 | ||||
| chr18:70205636-70205837 | Common:3; Rare:87; Clinvar (benign):2 | ||||
| chr18:70205979-70206153 | Rare:58 | ||||
| chr18:74148358-74148611 | Common:1; Rare:70 | ||||
| chr18:74291906-74292278 | Common:4; Rare:111 | ||||
| chr18:74496033-74496423 | Common:4; Rare:126 | ||||
| chr18:74499795-74499929 | Common:2; Rare:28 | ||||
| chr18:74597611-74597914 | Common:2; Rare:80 | ||||
| chr18:76822232-76822591 | Common:11; Rare:100 | ||||
| chr18:79988268-79988667 | Common:4; Rare:128; Clinvar:1; Clinvar (pathogenic):2 |