| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129284-36129563 | Common:1; Rare:91 | ||||
| chr18:36129702-36129993 | Common:2; Rare:109 | ||||
| chr18:36187419-36187545 | Common:3; Rare:53 | ||||
| chr18:36828251-36828296 | Rare:8 | ||||
| chr18:36828392-36828441 | Rare:11 | ||||
| chr18:36828739-36828920 | Rare:73 | ||||
| chr18:36828968-36829313 | Common:3; Rare:130 | ||||
| chr18:41954992-41955285 | Common:2; Rare:102 | ||||
| chr18:41955421-41955556 | Common:1; Rare:40 | ||||
| chr18:44679671-44679744 | Rare:14 | ||||
| chr18:44679752-44680171 | Common:1; Rare:54 | ||||
| chr18:45967218-45967521 | Common:1; Rare:111; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr18:46072235-46072318 | Common:1; Rare:18 | ||||
| chr18:46098040-46098180 | Common:2; Rare:49 | ||||
| chr18:46098202-46098377 | Common:11; Rare:80; Clinvar (benign):7 |