Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124791765-124791941 | Common:1; Rare:92 | ||||
chr10:125719453-125719780 | Common:1; Rare:123 | ||||
chr10:125823200-125823561 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905277-126905458 | Rare:68 | ||||
chr10:132331786-132332090 | Common:15; Rare:103 | ||||
chr10:133237668-133237858 | Rare:49 | ||||
chr10:133308837-133308998 | Rare:75 | ||||
chr11:207381-207526 | Common:4; Rare:55 | ||||
chr11:208662-208847 | Rare:70 | ||||
chr11:236340-236503 | Common:5; Rare:47 | ||||
chr11:236924-237052 | Common:1; Rare:50 | ||||
chr11:560718-561016 | Common:5; Rare:134 | ||||
chr11:747329-747510 | Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777471-777607 | Rare:59 | ||||
chr11:832879-833014 | Common:7; Rare:50 |