| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31943084-31943321 | Common:1; Rare:68 | ||||
| chr18:32092346-32092757 | Common:6; Rare:184 | ||||
| chr18:34976706-34977067 | Common:4; Rare:78 | ||||
| chr18:35240872-35241094 | Common:3; Rare:87 | ||||
| chr18:35290147-35290383 | Common:2; Rare:76 | ||||
| chr18:35344410-35344703 | Common:2; Rare:92 | ||||
| chr18:35972449-35972732 | Common:4; Rare:95 | ||||
| chr18:36067364-36067698 | Common:1; Rare:117 | ||||
| chr18:36129303-36129454 | Common:1; Rare:47 | ||||
| chr18:36129778-36129946 | Common:1; Rare:73 | ||||
| chr18:36159526-36159798 | Common:1; Rare:53 | ||||
| chr18:36187388-36187575 | Common:4; Rare:65 | ||||
| chr18:36828721-36829144 | Common:3; Rare:157 | ||||
| chr18:41955018-41955282 | Common:1; Rare:98 | ||||
| chr18:46098178-46098377 | Common:11; Rare:91; Clinvar (benign):8 |