| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23939188-23939663 | Common:2; Rare:115; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr18:23941270-23941669 | Common:6; Rare:70 | ||||
| chr18:23947750-23947799 | Rare:6 | ||||
| chr18:23960116-23960359 | Common:2; Rare:34 | ||||
| chr18:23961075-23961123 | Rare:8 | ||||
| chr18:24101323-24101487 | Rare:36 | ||||
| chr18:24170056-24170338 | Common:2; Rare:53 | ||||
| chr18:24171260-24171466 | Common:1; Rare:34 | ||||
| chr18:25988713-25988737 | Rare:4 | ||||
| chr18:26038449-26038647 | Common:1; Rare:49 | ||||
| chr18:26299256-26299290 | Rare:7 | ||||
| chr18:26310881-26310939 | Common:1; Rare:7 | ||||
| chr18:26545320-26545386 | Rare:14 | ||||
| chr18:26977226-26977421 | Rare:25 | ||||
| chr18:29156751-29156986 | Common:1; Rare:39 |