| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:34709232-34709374 | Common:1; Rare:17 | ||||
| chr18:34976966-34977061 | Common:1; Rare:11 | ||||
| chr18:35240917-35241109 | Common:2; Rare:71 | ||||
| chr18:35290172-35290397 | Common:2; Rare:78 | ||||
| chr18:35972452-35972731 | Common:4; Rare:95 | ||||
| chr18:36067361-36067681 | Common:1; Rare:109 | ||||
| chr18:36129229-36129551 | Common:4; Rare:105 | ||||
| chr18:36129772-36129934 | Common:1; Rare:64 | ||||
| chr18:36187414-36187534 | Common:2; Rare:46 | ||||
| chr18:36828746-36829259 | Common:3; Rare:201 | ||||
| chr18:44680664-44681018 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967261-45967477 | Rare:77 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46917385-46917647 | Common:2; Rare:111 | ||||
| chr18:47150433-47150570 | Common:4; Rare:52 |