| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36129735-36129960 | Common:1; Rare:90 | ||||
| chr18:36187419-36187559 | Common:4; Rare:55 | ||||
| chr18:36297544-36297742 | Common:3; Rare:76 | ||||
| chr18:36828576-36828909 | Rare:114 | ||||
| chr18:36828943-36829287 | Common:3; Rare:136 | ||||
| chr18:37253991-37254180 | Common:1; Rare:64 | ||||
| chr18:37566046-37566289 | Common:6; Rare:74 | ||||
| chr18:41954978-41955282 | Common:2; Rare:104 | ||||
| chr18:43277320-43277820 | Common:1; Rare:112 | ||||
| chr18:44680514-44680658 | Rare:36 | ||||
| chr18:44680779-44681196 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967261-45967556 | Common:1; Rare:105 | ||||
| chr18:46072251-46072383 | Common:1; Rare:28 | ||||
| chr18:46098258-46098667 | Common:11; Rare:104; Clinvar (benign):4 | ||||
| chr18:46104224-46104412 | Common:3; Rare:50 |