| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35972449-35972731 | Common:4; Rare:95 | ||||
| chr18:36129308-36129479 | Common:1; Rare:47 | ||||
| chr18:36129829-36129928 | Rare:41 | ||||
| chr18:36187336-36187584 | Common:4; Rare:81 | ||||
| chr18:36828742-36829148 | Common:3; Rare:155 | ||||
| chr18:45967243-45967508 | Rare:101 | ||||
| chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr18:47150452-47150570 | Common:3; Rare:43 | ||||
| chr18:49460448-49460466 | Rare:3 | ||||
| chr18:49487143-49487323 | Common:3; Rare:71 | ||||
| chr18:49561879-49562077 | Rare:51 | ||||
| chr18:49813489-49814308 | Common:3; Rare:270 | ||||
| chr18:50281426-50281602 | Common:2; Rare:61 | ||||
| chr18:50287634-50287765 | Rare:46 | ||||
| chr18:50374876-50375112 | Common:3; Rare:83 |