| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36187375-36187516 | Common:1; Rare:51 | ||||
| chr18:36828700-36829141 | Common:3; Rare:162 | ||||
| chr18:45967261-45967465 | Rare:74 | ||||
| chr18:46098214-46098396 | Common:11; Rare:77; Clinvar (benign):6 | ||||
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:47150444-47150546 | Common:2; Rare:37 | ||||
| chr18:49460621-49460804 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49487094-49487370 | Common:4; Rare:101 | ||||
| chr18:49490452-49490914 | Common:1; Rare:114 | ||||
| chr18:49561879-49562101 | Rare:58 | ||||
| chr18:49813826-49814080 | Common:1; Rare:109 | ||||
| chr18:49849804-49850039 | Common:2; Rare:58 | ||||
| chr18:50281436-50281565 | Rare:49 | ||||
| chr18:50374850-50375117 | Common:4; Rare:92 | ||||
| chr18:50878952-50879228 | Common:4; Rare:93 |