| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36187441-36187551 | Common:3; Rare:47 | ||||
| chr18:36828735-36829164 | Common:3; Rare:172 | ||||
| chr18:46098220-46098581 | Common:11; Rare:105; Clinvar (benign):6 | ||||
| chr18:46104135-46104426 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr18:46917355-46917639 | Common:3; Rare:126 | ||||
| chr18:47150452-47150575 | Common:3; Rare:45 | ||||
| chr18:48930275-48930449 | Common:1; Rare:38 | ||||
| chr18:48942526-48942747 | Common:1; Rare:71 | ||||
| chr18:49490452-49490914 | Common:1; Rare:114 | ||||
| chr18:49561896-49562098 | Rare:49 | ||||
| chr18:49813510-49813617 | Rare:22 | ||||
| chr18:49813826-49814128 | Common:1; Rare:126 | ||||
| chr18:50266438-50266660 | Common:1; Rare:86 | ||||
| chr18:50374876-50375137 | Common:3; Rare:85 | ||||
| chr18:50878954-50879219 | Common:4; Rare:90 |