| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:34978354-34978439 | Rare:16 | ||||
| chr18:35041221-35041459 | Common:2; Rare:85 | ||||
| chr18:35240898-35241143 | Common:2; Rare:91 | ||||
| chr18:35290184-35290389 | Common:2; Rare:72 | ||||
| chr18:35344376-35344529 | Common:2; Rare:48 | ||||
| chr18:35972449-35972739 | Common:4; Rare:98 | ||||
| chr18:36067387-36067699 | Common:1; Rare:111 | ||||
| chr18:36129117-36129479 | Common:4; Rare:103 | ||||
| chr18:36129772-36129939 | Common:1; Rare:68 | ||||
| chr18:36187371-36187568 | Common:4; Rare:68 | ||||
| chr18:36828715-36829280 | Common:3; Rare:217 | ||||
| chr18:45967261-45967465 | Rare:74 | ||||
| chr18:46098200-46098550 | Common:11; Rare:108; Clinvar (benign):7 | ||||
| chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr18:46173425-46173583 | Rare:40 |