Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:64245716-64245991 | Common:1; Rare:55 | ||||
chr11:64284643-64284867 | Common:1; Rare:100 | ||||
chr11:64317267-64317632 | Common:3; Rare:146 | ||||
chr11:64318003-64318345 | Common:1; Rare:149 | ||||
chr11:65084028-65084292 | Common:1; Rare:84 | ||||
chr11:65181594-65181980 | Common:3; Rare:111 | ||||
chr11:65333617-65333882 | Common:1; Rare:114 | ||||
chr11:65503080-65503402 | Rare:146 | ||||
chr11:65524824-65525126 | Rare:45 | ||||
chr11:65570359-65570510 | Rare:66 | ||||
chr11:65611011-65611445 | Rare:85 | ||||
chr11:65614180-65614419 | Rare:54 | ||||
chr11:65662886-65663008 | Common:1; Rare:34 | ||||
chr11:65919101-65919507 | Rare:142 | ||||
chr11:66002093-66002516 | Common:3; Rare:118; Clinvar:6; Clinvar (benign):3 |