| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129249-36129473 | Common:4; Rare:67 | ||||
| chr18:36129816-36129939 | Rare:54 | ||||
| chr18:36828772-36829132 | Common:3; Rare:132 | ||||
| chr18:46098244-46098598 | Common:11; Rare:97; Clinvar (benign):5 | ||||
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46173938-46174104 | Common:1; Rare:45 | ||||
| chr18:47150452-47150575 | Common:3; Rare:45 | ||||
| chr18:49460615-49460833 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49561883-49562093 | Rare:53 | ||||
| chr18:49813832-49814128 | Common:1; Rare:124 | ||||
| chr18:50374910-50375137 | Common:2; Rare:71 | ||||
| chr18:50878944-50879185 | Common:4; Rare:78 | ||||
| chr18:50967914-50968084 | Rare:59 | ||||
| chr18:54269410-54269618 | Common:2; Rare:94 | ||||
| chr18:54357838-54357973 | Common:5; Rare:42 |