| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:57586542-57587059 | Common:2; Rare:217; Clinvar (benign):2 | ||||
| chr18:57621696-57622074 | Common:9; Rare:305 | ||||
| chr18:57803012-57803600 | Common:10; Rare:303; Clinvar:1; Clinvar (benign):3 | ||||
| chr18:58043820-58044633 | Common:9; Rare:416 | ||||
| chr18:58045270-58045930 | Common:7; Rare:221 | ||||
| chr18:58090951-58091850 | Common:11; Rare:263 | ||||
| chr18:58195309-58195437 | Common:1; Rare:25 | ||||
| chr18:58221374-58221622 | Common:2; Rare:44 | ||||
| chr18:58671140-58671660 | Common:12; Rare:477; Clinvar:1; Clinvar (benign):2 | ||||
| chr18:59139439-59139560 | Rare:20 | ||||
| chr18:59139608-59139990 | Common:8; Rare:237 | ||||
| chr18:59358520-59358855 | Common:1; Rare:143 | ||||
| chr18:59359177-59359604 | Common:4; Rare:185; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:59899778-59900067 | Common:9; Rare:196 | ||||
| chr18:60372661-60373061 | Rare:163; Clinvar:2 |