| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:70590622-70590672 | Rare:7 | ||||
| chr12:70590695-70590927 | Rare:33 | ||||
| chr12:70591020-70591123 | Common:1; Rare:17 | ||||
| chr12:70599676-70599759 | Common:2; Rare:12 | ||||
| chr12:70600220-70600407 | Rare:35 | ||||
| chr12:70601247-70601432 | Common:1; Rare:38 | ||||
| chr12:70607141-70607481 | Common:1; Rare:60 | ||||
| chr12:70617485-70617596 | Rare:33 | ||||
| chr12:70617832-70617868 | Common:1; Rare:6 | ||||
| chr12:70618944-70619125 | Common:2; Rare:34 | ||||
| chr12:70622287-70622494 | Common:1; Rare:60 | ||||
| chr12:70634824-70634923 | Common:1; Rare:15 | ||||
| chr12:70636583-70636697 | Common:2; Rare:19 | ||||
| chr12:70661744-70662062 | Common:2; Rare:45 | ||||
| chr12:70691409-70691606 | Common:1; Rare:31 |