Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:17207889-17208093 | Common:2; Rare:80 | ||||
chr11:17276451-17276823 | Common:5; Rare:107; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr11:18012985-18013251 | Common:5; Rare:84 | ||||
chr11:18322113-18322610 | Common:8; Rare:180; Clinvar:1; Clinvar (benign):2 | ||||
chr11:18394432-18394608 | Common:1; Rare:70; Clinvar (benign):1 | ||||
chr11:18526889-18526994 | Rare:47 | ||||
chr11:18588672-18588884 | Common:2; Rare:71 | ||||
chr11:18634336-18634588 | Common:2; Rare:81 | ||||
chr11:19117002-19117189 | Common:1; Rare:45 | ||||
chr11:20363659-20363749 | Common:1; Rare:19 | ||||
chr11:20387431-20387730 | Common:7; Rare:93 | ||||
chr11:22625813-22626002 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
chr11:22674535-22674805 | Common:3; Rare:40 | ||||
chr11:27506748-27506875 | Common:1; Rare:53 | ||||
chr11:28108179-28108414 | Common:1; Rare:71 |