| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:32091842-32091997 | Common:3; Rare:58 | ||||
| chr18:32092116-32092235 | Common:2; Rare:25 | ||||
| chr18:32092388-32092756 | Common:5; Rare:163 | ||||
| chr18:35041176-35041460 | Common:2; Rare:92 | ||||
| chr18:35240900-35241109 | Common:2; Rare:79 | ||||
| chr18:35290188-35290391 | Common:2; Rare:72 | ||||
| chr18:35344383-35344765 | Common:2; Rare:108 | ||||
| chr18:35497595-35497710 | Common:3; Rare:45 | ||||
| chr18:35972449-35972785 | Common:4; Rare:118 | ||||
| chr18:36129079-36129479 | Common:4; Rare:113 | ||||
| chr18:36129753-36129939 | Common:1; Rare:73 | ||||
| chr18:36187350-36187568 | Common:4; Rare:74 | ||||
| chr18:36828731-36829280 | Common:3; Rare:214 | ||||
| chr18:45967243-45967531 | Common:1; Rare:108 | ||||
| chr18:46098200-46098598 | Common:11; Rare:120; Clinvar (benign):7 |