| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79069211-79069531 | Common:4; Rare:122 | ||||
| chr18:79679070-79679600 | Common:4; Rare:228 | ||||
| chr18:79679630-79679840 | Common:2; Rare:62 | ||||
| chr18:79679761-79679880 | Common:1; Rare:27 | ||||
| chr18:79951592-79951755 | Common:4; Rare:163 | ||||
| chr18:79964556-79964684 | Common:1; Rare:35 | ||||
| chr18:79988463-79988738 | Common:7; Rare:189; Clinvar (pathogenic):4 | ||||
| chr18:80033730-80034700 | Common:32; Rare:581 | ||||
| chr18:80108776-80109065 | Rare:70 | ||||
| chr19:291294-291670 | Common:15; Rare:126 | ||||
| chr19:344769-344925 | Common:6; Rare:83 | ||||
| chr19:488860-489192 | Common:16; Rare:175 | ||||
| chr19:506970-507250 | Common:2; Rare:73 | ||||
| chr19:507770-508090 | Common:7; Rare:163 | ||||
| chr19:531045-531226 | Common:2; Rare:45 |