| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36067296-36067716 | Common:2; Rare:139 | ||||
| chr18:36129114-36129479 | Common:4; Rare:103 | ||||
| chr18:36129772-36129934 | Common:1; Rare:64 | ||||
| chr18:36297606-36297978 | Common:3; Rare:137 | ||||
| chr18:36828683-36829177 | Common:3; Rare:193 | ||||
| chr18:37485782-37486003 | Rare:43 | ||||
| chr18:37565605-37565919 | Common:1; Rare:73 | ||||
| chr18:37565960-37566277 | Common:10; Rare:80 | ||||
| chr18:43115415-43115845 | Common:3; Rare:118 | ||||
| chr18:43115849-43115949 | Common:1; Rare:18 | ||||
| chr18:43277252-43277717 | Rare:113; Clinvar:1 | ||||
| chr18:44680659-44681004 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967261-45967517 | Rare:96 | ||||
| chr18:46097995-46098571 | Common:13; Rare:187; Clinvar (benign):8 | ||||
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 |