| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53321206-53321688 | Common:3; Rare:156; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr12:53324832-53325126 | Common:1; Rare:73 | ||||
| chr12:53325134-53325335 | Common:1; Rare:30 | ||||
| chr12:53344808-53344940 | Rare:30 | ||||
| chr12:53344961-53345170 | Common:2; Rare:31 | ||||
| chr12:53379941-53380206 | Common:1; Rare:102 | ||||
| chr12:53380366-53380501 | Rare:40 | ||||
| chr12:53380556-53380831 | Rare:92 | ||||
| chr12:53381034-53381068 | Common:1; Rare:7 | ||||
| chr12:53441162-53441413 | Common:1; Rare:48 | ||||
| chr12:53441425-53442090 | Common:1; Rare:180 | ||||
| chr12:53442550-53442691 | Rare:45 | ||||
| chr12:53451795-53452367 | Rare:129 | ||||
| chr12:53452439-53452695 | Common:1; Rare:88 | ||||
| chr12:53492921-53493296 | Common:4; Rare:101 |