| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21242058-21242434 | Common:1; Rare:134 | ||||
| chr18:21600210-21600291 | Common:1; Rare:14 | ||||
| chr18:21600292-21600488 | Common:1; Rare:58 | ||||
| chr18:21600589-21600978 | Common:2; Rare:104 | ||||
| chr18:21600999-21601142 | Rare:25 | ||||
| chr18:21612141-21612458 | Common:2; Rare:94 | ||||
| chr18:21612476-21612702 | Common:1; Rare:57 | ||||
| chr18:21703819-21704017 | Rare:64 | ||||
| chr18:21704384-21704563 | Common:1; Rare:47 | ||||
| chr18:21704677-21705018 | Common:3; Rare:108 | ||||
| chr18:21740571-21740915 | Common:3; Rare:105 | ||||
| chr18:21740952-21741543 | Common:3; Rare:153; Clinvar (benign):1 | ||||
| chr18:22169009-22169153 | Common:2; Rare:39 | ||||
| chr18:22169297-22169684 | Common:2; Rare:103 | ||||
| chr18:22169850-22169903 | Rare:12 |