| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600239-21600296 | Common:1; Rare:11 | ||||
| chr18:21600519-21600582 | Rare:20 | ||||
| chr18:21600606-21600926 | Common:2; Rare:86 | ||||
| chr18:21612116-21612702 | Common:3; Rare:159 | ||||
| chr18:21703671-21703894 | Rare:73 | ||||
| chr18:21704260-21704426 | Common:1; Rare:43 | ||||
| chr18:21704661-21705022 | Common:3; Rare:112 | ||||
| chr18:21740569-21741170 | Common:5; Rare:172 | ||||
| chr18:21741184-21741404 | Common:1; Rare:52 | ||||
| chr18:22169311-22169604 | Common:2; Rare:80 | ||||
| chr18:22932912-22933009 | Rare:18 | ||||
| chr18:22933124-22933467 | Common:4; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933508-22933622 | Common:1; Rare:24; Clinvar:2 | ||||
| chr18:22933635-22933927 | Common:2; Rare:105 | ||||
| chr18:23134507-23134570 | Rare:8 |