| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46098244-46098598 | Common:11; Rare:97; Clinvar (benign):5 | ||||
| chr18:46104135-46104423 | Common:4; Rare:88; Clinvar (benign):1 | ||||
| chr18:46173425-46173557 | Rare:34 | ||||
| chr18:46173895-46174104 | Common:1; Rare:53 | ||||
| chr18:46333776-46334015 | Common:2; Rare:65 | ||||
| chr18:47150425-47150589 | Common:4; Rare:68 | ||||
| chr18:47176273-47176437 | Common:1; Rare:74; Clinvar (benign):1 | ||||
| chr18:48538922-48539287 | Common:2; Rare:81 | ||||
| chr18:49460599-49460762 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49487049-49487328 | Common:3; Rare:107 | ||||
| chr18:49490452-49490935 | Common:1; Rare:119 | ||||
| chr18:49492246-49492565 | Common:2; Rare:126 | ||||
| chr18:49813485-49813641 | Rare:37 | ||||
| chr18:49813815-49814158 | Common:1; Rare:139 | ||||
| chr18:50266472-50266666 | Common:1; Rare:66 |