Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:120851209-120851406 | Common:4; Rare:67 | ||||
chr10:122954188-122954474 | Rare:105 | ||||
chr10:123008790-123009032 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125823200-125823577 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905309-126905452 | Rare:54 | ||||
chr10:131981904-131982143 | Common:1; Rare:86 | ||||
chr10:133308829-133308961 | Rare:62 | ||||
chr11:207363-207734 | Common:7; Rare:115 | ||||
chr11:208638-208847 | Rare:76 | ||||
chr11:236232-236485 | Common:7; Rare:92 | ||||
chr11:236720-237022 | Common:3; Rare:90 | ||||
chr11:320686-320936 | Common:5; Rare:99; Clinvar:1 | ||||
chr11:560698-560987 | Common:6; Rare:133 | ||||
chr11:706517-706663 | Rare:29 | ||||
chr11:777465-777614 | Common:1; Rare:65 |