| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:24397768-24398102 | Common:2; Rare:120 | ||||
| chr18:24426593-24426781 | Common:3; Rare:73 | ||||
| chr18:26091123-26091299 | Common:2; Rare:46 | ||||
| chr18:31042485-31042605 | Common:1; Rare:39 | ||||
| chr18:31042639-31043084 | Common:3; Rare:91 | ||||
| chr18:31101919-31102031 | Common:1; Rare:29; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31102285-31102393 | Rare:27; Clinvar:3 | ||||
| chr18:31498011-31498284 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):6 | ||||
| chr18:32092384-32092706 | Common:4; Rare:146 | ||||
| chr18:35041269-35041418 | Rare:51 | ||||
| chr18:35240917-35241069 | Common:2; Rare:52 | ||||
| chr18:35290193-35290389 | Common:2; Rare:69 | ||||
| chr18:35972462-35972736 | Common:3; Rare:93 | ||||
| chr18:36129254-36129471 | Common:3; Rare:64 | ||||
| chr18:36129788-36129928 | Common:1; Rare:54 |