| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134223911-134224103 | Common:2; Rare:61 | ||||
| chr11:134224533-134224680 | Rare:52 | ||||
| chr11:134253261-134253597 | Common:2; Rare:113; Clinvar (benign):1 | ||||
| chr11:134276152-134276364 | Common:3; Rare:44 | ||||
| chr12:389249-389383 | Rare:51 | ||||
| chr12:389449-389687 | Common:5; Rare:100 | ||||
| chr12:401436-401691 | Rare:71 | ||||
| chr12:752286-752602 | Common:1; Rare:91 | ||||
| chr12:949493-949537 | Common:1; Rare:10 | ||||
| chr12:949547-949844 | Common:6; Rare:87 | ||||
| chr12:991080-991322 | Common:4; Rare:110 | ||||
| chr12:1690866-1691174 | Common:2; Rare:113 | ||||
| chr12:2004420-2004669 | Common:2; Rare:80 | ||||
| chr12:2812432-2812763 | Common:1; Rare:90 | ||||
| chr12:2812878-2812956 | Rare:29 |