| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57110292-57110633 | Common:1; Rare:71 | ||||
| chr12:57111339-57111669 | Common:1; Rare:56 | ||||
| chr12:57229577-57229790 | Common:3; Rare:89 | ||||
| chr12:57230155-57230229 | Rare:13 | ||||
| chr12:57233572-57233844 | Common:1; Rare:85 | ||||
| chr12:57240366-57240660 | Rare:57 | ||||
| chr12:57430747-57431051 | Common:1; Rare:73 | ||||
| chr12:57454972-57455310 | Rare:65 | ||||
| chr12:57488796-57489037 | Common:3; Rare:49; Clinvar (benign):1 | ||||
| chr12:57520473-57520714 | Common:2; Rare:78 | ||||
| chr12:57549744-57550095 | Rare:77 | ||||
| chr12:57591108-57591282 | Common:4; Rare:80 | ||||
| chr12:57604446-57604845 | Common:1; Rare:69 | ||||
| chr12:57611226-57611467 | Rare:50 | ||||
| chr12:57611594-57611984 | Common:3; Rare:106 |