Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:103396462-103396659 | Rare:70 | ||||
chr10:110006005-110006063 | Common:2; Rare:20 | ||||
chr10:110919332-110919615 | Common:7; Rare:72 | ||||
chr10:120851207-120851387 | Common:4; Rare:55 | ||||
chr10:123008786-123009006 | Common:5; Rare:60; Clinvar:3; Clinvar (benign):5 | ||||
chr10:125823226-125823563 | Rare:107; Clinvar:1 | ||||
chr10:133308829-133308961 | Rare:62 | ||||
chr11:207252-207526 | Common:8; Rare:115 | ||||
chr11:706517-706645 | Rare:21 | ||||
chr11:842500-842942 | Common:8; Rare:184 | ||||
chr11:843871-844104 | Common:2; Rare:67 | ||||
chr11:1309613-1309763 | Common:1; Rare:69 | ||||
chr11:6481304-6481519 | Common:3; Rare:85 | ||||
chr11:6603614-6603811 | Common:2; Rare:61; Clinvar (benign):3 | ||||
chr11:8682660-8682792 | Common:2; Rare:52 |