| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:133946524-133946803 | Common:1; Rare:60 | ||||
| chr11:133952020-133952173 | Rare:58 | ||||
| chr11:134253225-134253594 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr12:262816-263008 | Rare:33 | ||||
| chr12:389242-389383 | Rare:53 | ||||
| chr12:389533-389680 | Common:5; Rare:69 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:752269-752602 | Common:1; Rare:98 | ||||
| chr12:949617-949849 | Common:4; Rare:70 | ||||
| chr12:990431-990595 | Common:1; Rare:42 | ||||
| chr12:991080-991321 | Common:4; Rare:109 | ||||
| chr12:2004427-2004680 | Common:2; Rare:79 | ||||
| chr12:2794865-2795169 | Common:1; Rare:106 | ||||
| chr12:2812516-2812714 | Common:1; Rare:48 | ||||
| chr12:2812880-2813057 | Rare:50 |