| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600458-21600559 | Rare:25 | ||||
| chr18:21600629-21600931 | Common:2; Rare:80 | ||||
| chr18:21600933-21601221 | Rare:61 | ||||
| chr18:21704648-21704984 | Common:3; Rare:106 | ||||
| chr18:21740609-21740861 | Common:2; Rare:82 | ||||
| chr18:21741780-21741805 | Rare:6; Clinvar (benign):1 | ||||
| chr18:22168761-22169124 | Common:5; Rare:78 | ||||
| chr18:22169287-22169682 | Common:2; Rare:107 | ||||
| chr18:22169824-22169993 | Common:1; Rare:33 | ||||
| chr18:22913908-22914161 | Rare:41 | ||||
| chr18:22933324-22933454 | Common:2; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933742-22933902 | Common:1; Rare:66 | ||||
| chr18:23453172-23453376 | Rare:69 | ||||
| chr18:23503293-23503650 | Common:4; Rare:154 | ||||
| chr18:23529827-23530109 | Common:3; Rare:62 |