| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253273-134253601 | Common:2; Rare:114; Clinvar (benign):1 | ||||
| chr11:134331689-134332023 | Common:10; Rare:74 | ||||
| chr12:389249-389360 | Rare:39 | ||||
| chr12:389537-389662 | Common:5; Rare:56 | ||||
| chr12:401420-401655 | Common:2; Rare:67 | ||||
| chr12:914256-914281 | Rare:3 | ||||
| chr12:949510-949776 | Common:7; Rare:79 | ||||
| chr12:990775-990873 | Rare:30 | ||||
| chr12:991101-991322 | Common:3; Rare:100 | ||||
| chr12:1690871-1691076 | Common:2; Rare:75 | ||||
| chr12:2004427-2004629 | Common:1; Rare:71 | ||||
| chr12:2794939-2795203 | Rare:105 | ||||
| chr12:2796965-2797211 | Rare:63 | ||||
| chr12:2812522-2812735 | Common:1; Rare:57 | ||||
| chr12:2812885-2812998 | Rare:36 |