Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:125451479-125451625 | Rare:30 | ||||
chr11:125592597-125592913 | Common:6; Rare:101 | ||||
chr11:125625874-125625912 | Rare:17 | ||||
chr11:126211634-126211817 | Rare:83 | ||||
chr11:126268802-126269207 | Common:2; Rare:159; Clinvar:2; Clinvar (benign):4 | ||||
chr11:126282928-126283124 | Common:2; Rare:63 | ||||
chr11:126355526-126355778 | Common:2; Rare:71 | ||||
chr11:128693803-128694162 | Common:2; Rare:69 | ||||
chr11:130314406-130314519 | Common:1; Rare:37 | ||||
chr11:130448414-130448652 | Rare:58 | ||||
chr11:134224539-134224685 | Rare:51 | ||||
chr11:134225435-134225461 | Rare:8 | ||||
chr11:134253299-134253602 | Common:2; Rare:105; Clinvar (benign):1 | ||||
chr12:389249-389347 | Rare:38 | ||||
chr12:401446-401655 | Rare:55 |