| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21111516-21111938 | Common:2; Rare:129 | ||||
| chr18:21600644-21600931 | Common:2; Rare:77 | ||||
| chr18:21704662-21704984 | Common:3; Rare:103 | ||||
| chr18:22168894-22169138 | Common:3; Rare:52 | ||||
| chr18:22169299-22169595 | Common:2; Rare:83 | ||||
| chr18:22169853-22169943 | Rare:17 | ||||
| chr18:22170667-22170983 | Common:1; Rare:60 | ||||
| chr18:22933280-22933426 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933781-22933912 | Common:1; Rare:54 | ||||
| chr18:23453064-23453353 | Rare:100 | ||||
| chr18:23503308-23503576 | Common:2; Rare:100 | ||||
| chr18:23586354-23586531 | Common:4; Rare:74; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:23586876-23587060 | Common:1; Rare:61 | ||||
| chr18:24397784-24398076 | Common:2; Rare:109 | ||||
| chr18:24426620-24426785 | Common:3; Rare:64 |