| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45727811-45727839 | Rare:6 | ||||
| chr12:45730858-45731054 | Common:1; Rare:31 | ||||
| chr12:46383494-46383690 | Common:2; Rare:53 | ||||
| chr12:48198127-48198379 | Common:4; Rare:64 | ||||
| chr12:49234554-49234705 | Common:1; Rare:45 | ||||
| chr12:52032939-52033237 | Common:1; Rare:86 | ||||
| chr12:53750791-53750947 | Rare:39 | ||||
| chr12:54359001-54359471 | Common:3; Rare:109 | ||||
| chr12:56190248-56190330 | Common:1; Rare:45 | ||||
| chr12:56634993-56635096 | Rare:16 | ||||
| chr12:57211946-57212223 | Common:1; Rare:70 | ||||
| chr12:57239137-57239416 | Common:1; Rare:63 | ||||
| chr12:57243247-57243257 | Rare:3 | ||||
| chr12:57245143-57245292 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr12:57462785-57463078 | Common:2; Rare:56 |