| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22933221-22933454 | Common:11; Rare:312; Clinvar:14; Clinvar (benign):8 | ||||
| chr18:22933460-22933650 | Common:3; Rare:54; Clinvar:5; Clinvar (benign):1 | ||||
| chr18:22933670-22934180 | Common:9; Rare:530 | ||||
| chr18:23437187-23437805 | Common:4; Rare:182 | ||||
| chr18:23437792-23438251 | Common:14; Rare:340 | ||||
| chr18:23453014-23453414 | Rare:525 | ||||
| chr18:23502715-23503200 | Common:2; Rare:149 | ||||
| chr18:23503220-23503630 | Common:20; Rare:844 | ||||
| chr18:23503615-23504015 | Common:4; Rare:183 | ||||
| chr18:23528777-23529177 | Rare:103 | ||||
| chr18:23529602-23530002 | Common:4; Rare:115 | ||||
| chr18:23534493-23534893 | Common:1; Rare:88; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr18:23585519-23586105 | Rare:116 | ||||
| chr18:23586250-23586803 | Common:18; Rare:641; Clinvar:28; Clinvar (benign):12 | ||||
| chr18:23586821-23587221 | Common:5; Rare:251 |