| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130448379-130448654 | Rare:68 | ||||
| chr11:130916435-130916661 | Common:5; Rare:64 | ||||
| chr11:134223922-134224166 | Common:2; Rare:80 | ||||
| chr11:134224530-134224680 | Rare:53 | ||||
| chr11:134253273-134253601 | Common:2; Rare:114; Clinvar (benign):1 | ||||
| chr12:389216-389350 | Rare:51 | ||||
| chr12:401426-401675 | Common:1; Rare:71 | ||||
| chr12:752311-752587 | Common:1; Rare:82 | ||||
| chr12:991095-991248 | Common:1; Rare:59 | ||||
| chr12:1629122-1629246 | Rare:21 | ||||
| chr12:1629744-1629922 | Common:1; Rare:41 | ||||
| chr12:1918617-1918842 | Common:1; Rare:41; Clinvar:2 | ||||
| chr12:2004430-2004666 | Common:2; Rare:73 | ||||
| chr12:2812495-2812752 | Common:1; Rare:72 | ||||
| chr12:2812891-2813057 | Rare:44 |