| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35240917-35241094 | Common:2; Rare:66 | ||||
| chr18:35290178-35290432 | Common:3; Rare:89 | ||||
| chr18:35972342-35972740 | Common:4; Rare:133 | ||||
| chr18:36129254-36129525 | Common:3; Rare:83 | ||||
| chr18:36129772-36129939 | Common:1; Rare:68 | ||||
| chr18:36187356-36187546 | Common:3; Rare:70 | ||||
| chr18:36828748-36829183 | Common:3; Rare:173 | ||||
| chr18:44680696-44681006 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967229-45967508 | Rare:104; Clinvar (pathogenic):1 | ||||
| chr18:46072240-46072356 | Rare:23 | ||||
| chr18:46087006-46087448 | Rare:92; Clinvar (pathogenic):2 | ||||
| chr18:46098175-46098550 | Common:11; Rare:120; Clinvar (benign):8 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46917370-46917659 | Common:3; Rare:123 | ||||
| chr18:47150446-47150546 | Common:2; Rare:36 |