| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600020-21600420 | Common:4; Rare:188 | ||||
| chr18:21600427-21601300 | Common:5; Rare:384 | ||||
| chr18:21612153-21612421 | Common:2; Rare:154 | ||||
| chr18:21704558-21705001 | Common:4; Rare:217 | ||||
| chr18:21740592-21740906 | Common:5; Rare:178 | ||||
| chr18:21740920-21741367 | Common:4; Rare:151 | ||||
| chr18:22169311-22169624 | Common:4; Rare:158 | ||||
| chr18:22170010-22170750 | Common:4; Rare:259 | ||||
| chr18:22933751-22933907 | Common:2; Rare:123 | ||||
| chr18:23135328-23135492 | Common:3; Rare:71 | ||||
| chr18:23135880-23136465 | Common:12; Rare:268 | ||||
| chr18:23453165-23453353 | Rare:117 | ||||
| chr18:23503293-23503561 | Common:4; Rare:191 | ||||
| chr18:23559987-23560799 | Common:7; Rare:330; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr18:23586369-23586561 | Common:5; Rare:166; Clinvar:9; Clinvar (benign):3 |