| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:48539937-48540032 | Rare:10 | ||||
| chr18:49460583-49460836 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:49487143-49487361 | Common:4; Rare:90 | ||||
| chr18:49491813-49491962 | Common:1; Rare:46 | ||||
| chr18:49561890-49562093 | Rare:49 | ||||
| chr18:49813469-49813617 | Rare:35 | ||||
| chr18:49813751-49814246 | Common:1; Rare:190 | ||||
| chr18:49849828-49850003 | Rare:43 | ||||
| chr18:50281423-50281549 | Rare:51 | ||||
| chr18:50374876-50375071 | Common:2; Rare:69 | ||||
| chr18:50878923-50879254 | Common:4; Rare:111 | ||||
| chr18:50967915-50968086 | Rare:59 | ||||
| chr18:51030064-51030252 | Rare:64; Clinvar:1 | ||||
| chr18:54269346-54269793 | Common:6; Rare:158 | ||||
| chr18:54357818-54357903 | Common:3; Rare:30 |