| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53344824-53345598 | Common:8; Rare:210 | ||||
| chr12:53379411-53380396 | Common:18; Rare:1131 | ||||
| chr12:53380480-53380912 | Common:1; Rare:409 | ||||
| chr12:53423856-53424401 | Common:3; Rare:147 | ||||
| chr12:53424848-53425248 | Common:3; Rare:165; Clinvar (pathogenic):1 | ||||
| chr12:53425528-53425932 | Common:2; Rare:222; Clinvar (benign):2 | ||||
| chr12:53440912-53441329 | Common:5; Rare:106 | ||||
| chr12:53441350-53441893 | Common:7; Rare:715 | ||||
| chr12:53451791-53452359 | Rare:318 | ||||
| chr12:53452361-53453060 | Common:8; Rare:638 | ||||
| chr12:53492870-53493849 | Common:12; Rare:586 | ||||
| chr12:53494065-53494465 | Rare:101 | ||||
| chr12:53499289-53499709 | Rare:256 | ||||
| chr12:53500619-53501234 | Common:19; Rare:532 | ||||
| chr12:53501166-53501376 | Rare:132 |