| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:33578320-33578539 | Common:3; Rare:55 | ||||
| chr18:34976916-34977079 | Common:1; Rare:30 | ||||
| chr18:35240917-35241129 | Common:2; Rare:80 | ||||
| chr18:35290145-35290397 | Common:2; Rare:81 | ||||
| chr18:35344377-35344524 | Common:2; Rare:46 | ||||
| chr18:35377300-35377404 | Common:2; Rare:27 | ||||
| chr18:35972472-35972731 | Common:3; Rare:89 | ||||
| chr18:36067312-36067761 | Common:2; Rare:147 | ||||
| chr18:36129223-36129551 | Common:4; Rare:107 | ||||
| chr18:36129772-36129936 | Common:1; Rare:66 | ||||
| chr18:36187362-36187530 | Common:2; Rare:60 | ||||
| chr18:36828736-36829244 | Common:3; Rare:202 | ||||
| chr18:44680696-44681018 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967231-45967477 | Rare:88; Clinvar (pathogenic):1 | ||||
| chr18:46098175-46098427 | Common:11; Rare:103; Clinvar (benign):8 |