Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65354527-65354757 | Common:1; Rare:61 | ||||
chr11:65502658-65503334 | Common:1; Rare:299 | ||||
chr11:65503348-65503409 | Rare:30 | ||||
chr11:65503618-65504113 | Common:1; Rare:247 | ||||
chr11:65524831-65525149 | Rare:55 | ||||
chr11:65525351-65525517 | Rare:34 | ||||
chr11:65557744-65558033 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
chr11:65570335-65570511 | Rare:72 | ||||
chr11:65575910-65576071 | Common:3; Rare:50 | ||||
chr11:65614186-65614393 | Rare:44 | ||||
chr11:65615245-65615841 | Common:3; Rare:212 | ||||
chr11:65616044-65616190 | Rare:43 | ||||
chr11:65637964-65638147 | Common:3; Rare:79 | ||||
chr11:65642144-65642327 | Rare:49 | ||||
chr11:65647065-65647416 | Common:3; Rare:96 |