Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124092724-124092828 | Rare:28 | ||||
chr10:124461711-124461868 | Common:4; Rare:57 | ||||
chr10:124791834-124791984 | Rare:74 | ||||
chr10:125719453-125719718 | Rare:81 | ||||
chr10:125823200-125823573 | Common:1; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
chr10:132332244-132332310 | Rare:16 | ||||
chr10:133276837-133277002 | Rare:40 | ||||
chr10:133308835-133308968 | Rare:63 | ||||
chr10:133393968-133394323 | Common:2; Rare:154 | ||||
chr11:207343-207729 | Common:8; Rare:132 | ||||
chr11:208617-208847 | Rare:81 | ||||
chr11:236314-236546 | Common:8; Rare:81 | ||||
chr11:236918-237019 | Rare:38 | ||||
chr11:288827-289174 | Common:3; Rare:95 | ||||
chr11:308104-308337 | Common:5; Rare:81 |