| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600629-21600938 | Common:2; Rare:81 | ||||
| chr18:22168907-22169032 | Common:2; Rare:19 | ||||
| chr18:22169321-22169617 | Common:2; Rare:78 | ||||
| chr18:22170674-22170902 | Common:1; Rare:40 | ||||
| chr18:22933260-22933413 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr18:22933777-22933903 | Common:1; Rare:50 | ||||
| chr18:23453172-23453370 | Rare:68 | ||||
| chr18:23503293-23503621 | Common:4; Rare:139 | ||||
| chr18:23529827-23530115 | Common:3; Rare:63 | ||||
| chr18:23586360-23586541 | Common:4; Rare:77; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:23586884-23587186 | Common:2; Rare:85 | ||||
| chr18:23992608-23992923 | Common:1; Rare:56 | ||||
| chr18:24397674-24398086 | Common:2; Rare:135 | ||||
| chr18:24426600-24426765 | Common:3; Rare:66 | ||||
| chr18:25231502-25231603 | Rare:19 |