| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46104136-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:46173982-46174140 | Common:1; Rare:37 | ||||
| chr18:49487156-49487323 | Common:2; Rare:62 | ||||
| chr18:49813891-49814273 | Common:1; Rare:165 | ||||
| chr18:50878921-50879228 | Common:4; Rare:105 | ||||
| chr18:51030054-51030226 | Rare:56 | ||||
| chr18:54269467-54269617 | Common:2; Rare:77 | ||||
| chr18:54357848-54357903 | Common:1; Rare:18 | ||||
| chr18:55422309-55422624 | Common:1; Rare:54 | ||||
| chr18:55589713-55589996 | Common:2; Rare:92 | ||||
| chr18:56651133-56651379 | Common:3; Rare:62 | ||||
| chr18:56651610-56651701 | Common:3; Rare:20 | ||||
| chr18:57688486-57688709 | Common:2; Rare:35; Clinvar:1 | ||||
| chr18:58221371-58221618 | Common:1; Rare:45 | ||||
| chr18:59359223-59359517 | Common:3; Rare:131; Clinvar:1 |