| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79679276-79679654 | Common:2; Rare:181 | ||||
| chr18:79679680-79679883 | Common:2; Rare:64 | ||||
| chr18:79951586-79951859 | Common:4; Rare:121 | ||||
| chr18:79964534-79964647 | Common:1; Rare:42 | ||||
| chr18:79988524-79988725 | Common:3; Rare:82; Clinvar (pathogenic):2 | ||||
| chr18:80034165-80034538 | Common:6; Rare:146 | ||||
| chr18:80034597-80034997 | Common:2; Rare:129 | ||||
| chr18:80108780-80109090 | Common:1; Rare:74 | ||||
| chr18:80109110-80109380 | Common:1; Rare:85 | ||||
| chr18:80109697-80110014 | Common:1; Rare:80 | ||||
| chr18:80247024-80247134 | Rare:43 | ||||
| chr18:80247380-80247740 | Common:1; Rare:100 | ||||
| chr19:344769-344967 | Common:3; Rare:71 | ||||
| chr19:408612-409012 | Common:2; Rare:162 | ||||
| chr19:409145-409344 | Common:2; Rare:67 |