| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54281195-54281502 | Common:3; Rare:92 | ||||
| chr12:54282594-54282874 | Rare:92 | ||||
| chr12:54300854-54301144 | Rare:55 | ||||
| chr12:54324797-54325172 | Rare:87 | ||||
| chr12:54384684-54384746 | Rare:6 | ||||
| chr12:54385731-54385905 | Rare:34 | ||||
| chr12:54391245-54391443 | Rare:47 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:54561182-54561491 | Common:1; Rare:48 | ||||
| chr12:54984661-54984823 | Rare:29 | ||||
| chr12:55712110-55712231 | Common:4; Rare:32 | ||||
| chr12:55715998-55716531 | Common:3; Rare:177 | ||||
| chr12:55720201-55720430 | Common:3; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:55725850-55726190 | Rare:70 | ||||
| chr12:55728275-55728521 | Rare:77 |