| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:62186886-62187320 | Common:5; Rare:120 | ||||
| chr18:62187736-62188022 | Common:1; Rare:77 | ||||
| chr18:62325187-62325355 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr18:62522844-62523025 | Common:3; Rare:60 | ||||
| chr18:62523078-62523330 | Rare:93 | ||||
| chr18:62715135-62715482 | Common:3; Rare:97 | ||||
| chr18:62715492-62715552 | Rare:20 | ||||
| chr18:63367009-63367056 | Rare:9 | ||||
| chr18:63367158-63367317 | Common:1; Rare:54 | ||||
| chr18:63367518-63367659 | Common:6; Rare:47 | ||||
| chr18:63422343-63422598 | Rare:75 | ||||
| chr18:63970444-63970494 | Rare:16 | ||||
| chr18:67516705-67517033 | Common:5; Rare:85 | ||||
| chr18:68714974-68715364 | Common:7; Rare:156 | ||||
| chr18:70205644-70205787 | Common:3; Rare:59; Clinvar (benign):2 |