| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23453172-23453312 | Rare:39 | ||||
| chr18:23586402-23586532 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:26133837-26133901 | Rare:17 | ||||
| chr18:26226230-26226481 | Common:3; Rare:89 | ||||
| chr18:31943069-31943424 | Common:7; Rare:118 | ||||
| chr18:32018748-32018860 | Common:1; Rare:31 | ||||
| chr18:32091740-32091924 | Common:4; Rare:64 | ||||
| chr18:32092338-32092733 | Common:6; Rare:177 | ||||
| chr18:35240917-35241112 | Common:2; Rare:71 | ||||
| chr18:35290162-35290377 | Common:2; Rare:73 | ||||
| chr18:35497886-35497972 | Common:1; Rare:34 | ||||
| chr18:35498013-35498178 | Common:1; Rare:32 | ||||
| chr18:36129788-36129931 | Common:1; Rare:56 | ||||
| chr18:36828772-36828879 | Rare:36 | ||||
| chr18:45967265-45967498 | Rare:82 |