| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253306-134253594 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:389249-389391 | Common:1; Rare:53 | ||||
| chr12:389481-389662 | Common:5; Rare:75 | ||||
| chr12:401438-401664 | Rare:62 | ||||
| chr12:991101-991316 | Common:3; Rare:98 | ||||
| chr12:2004420-2004669 | Common:2; Rare:80 | ||||
| chr12:2812516-2812748 | Common:1; Rare:67 | ||||
| chr12:2812878-2813036 | Rare:46 | ||||
| chr12:2877022-2877262 | Rare:71 | ||||
| chr12:2890706-2890935 | Common:1; Rare:89 | ||||
| chr12:3873355-3873574 | Common:2; Rare:51 | ||||
| chr12:4275420-4275703 | Common:3; Rare:48 | ||||
| chr12:4275749-4276046 | Rare:64 | ||||
| chr12:4320943-4321266 | Common:5; Rare:125 | ||||
| chr12:4538440-4538934 | Common:3; Rare:111 |