| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35290193-35290391 | Common:2; Rare:71 | ||||
| chr18:35344394-35344529 | Common:2; Rare:42 | ||||
| chr18:35972472-35972750 | Common:3; Rare:99 | ||||
| chr18:36067361-36067666 | Common:1; Rare:108 | ||||
| chr18:36129219-36129500 | Common:4; Rare:85 | ||||
| chr18:36129845-36129935 | Rare:40 | ||||
| chr18:36187428-36187534 | Common:2; Rare:45 | ||||
| chr18:36828748-36829140 | Common:3; Rare:145 | ||||
| chr18:45967261-45967513 | Rare:95 | ||||
| chr18:46087071-46087458 | Rare:90; Clinvar (pathogenic):2 | ||||
| chr18:46098175-46098647 | Common:11; Rare:145; Clinvar (benign):8 | ||||
| chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr18:47150452-47150619 | Common:3; Rare:72 | ||||
| chr18:49460607-49460902 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49487174-49487361 | Common:3; Rare:74 |