| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:32091863-32091969 | Common:3; Rare:39 | ||||
| chr18:32092416-32092727 | Common:4; Rare:143 | ||||
| chr18:33578316-33578649 | Common:3; Rare:87 | ||||
| chr18:35041250-35041467 | Common:1; Rare:82 | ||||
| chr18:35240917-35241090 | Common:2; Rare:64 | ||||
| chr18:35290145-35290384 | Common:2; Rare:76 | ||||
| chr18:35344394-35344529 | Common:2; Rare:42 | ||||
| chr18:35377280-35377406 | Common:2; Rare:33 | ||||
| chr18:35972449-35972719 | Common:4; Rare:85 | ||||
| chr18:36067328-36067722 | Common:2; Rare:135 | ||||
| chr18:36129173-36129525 | Common:4; Rare:106 | ||||
| chr18:36129845-36129934 | Rare:39 | ||||
| chr18:36187377-36187565 | Common:4; Rare:66 | ||||
| chr18:36828736-36829227 | Common:3; Rare:196 | ||||
| chr18:44680696-44681015 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):1 |