| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22933141-22933426 | Common:4; Rare:99; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933777-22933889 | Common:1; Rare:43 | ||||
| chr18:23453069-23453386 | Rare:108 | ||||
| chr18:23503291-23503640 | Common:4; Rare:151 | ||||
| chr18:23529827-23530049 | Common:3; Rare:42 | ||||
| chr18:23586291-23586537 | Common:4; Rare:101; Clinvar:7; Clinvar (benign):3 | ||||
| chr18:23586871-23587083 | Common:1; Rare:70 | ||||
| chr18:23689326-23689432 | Rare:31 | ||||
| chr18:24397778-24397933 | Common:1; Rare:66 | ||||
| chr18:24426620-24426759 | Common:3; Rare:60 | ||||
| chr18:25351041-25351133 | Rare:32 | ||||
| chr18:26090071-26090209 | Rare:55 | ||||
| chr18:26090576-26090689 | Common:1; Rare:54 | ||||
| chr18:26226240-26226455 | Common:1; Rare:68 | ||||
| chr18:26546938-26547166 | Rare:73 |