| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13726488-13726720 | Common:3; Rare:88 | ||||
| chr18:22169321-22169435 | Common:2; Rare:29 | ||||
| chr18:23453156-23453341 | Rare:66 | ||||
| chr18:23586416-23586535 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24397788-24398088 | Common:2; Rare:110 | ||||
| chr18:24426583-24426749 | Common:3; Rare:71 | ||||
| chr18:25352104-25352431 | Common:2; Rare:131 | ||||
| chr18:31318018-31318157 | Rare:19 | ||||
| chr18:32092378-32092688 | Common:4; Rare:140 | ||||
| chr18:35240917-35241055 | Common:2; Rare:45 | ||||
| chr18:35290193-35290377 | Common:2; Rare:67 | ||||
| chr18:36129301-36129508 | Common:1; Rare:62 | ||||
| chr18:36187408-36187592 | Common:4; Rare:65 | ||||
| chr18:36828765-36829141 | Common:3; Rare:138 | ||||
| chr18:46104135-46104399 | Common:3; Rare:75; Clinvar (benign):1 |