| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31498063-31498259 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:31943095-31943375 | Common:7; Rare:90 | ||||
| chr18:32092378-32092754 | Common:5; Rare:169 | ||||
| chr18:34976942-34977058 | Common:1; Rare:20 | ||||
| chr18:35041227-35041541 | Common:2; Rare:116 | ||||
| chr18:35290183-35290391 | Common:2; Rare:75 | ||||
| chr18:35972462-35972777 | Common:3; Rare:113 | ||||
| chr18:36067376-36067666 | Common:1; Rare:102 | ||||
| chr18:36129254-36129479 | Common:3; Rare:66 | ||||
| chr18:36129772-36129934 | Common:1; Rare:64 | ||||
| chr18:36828748-36829148 | Common:3; Rare:148 | ||||
| chr18:44680740-44681006 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967247-45967451 | Rare:75 | ||||
| chr18:46098220-46098550 | Common:11; Rare:98; Clinvar (benign):6 | ||||
| chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 |