Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:34105302-34105784 | Common:4; Rare:144 | ||||
chr11:34916292-34916709 | Common:10; Rare:171; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:35139018-35139177 | Common:1; Rare:33 | ||||
chr11:35943939-35944110 | Common:2; Rare:58 | ||||
chr11:36510236-36510396 | Rare:51 | ||||
chr11:43358799-43358983 | Rare:88 | ||||
chr11:46120952-46121259 | Common:2; Rare:46 | ||||
chr11:46345314-46345469 | Common:1; Rare:58 | ||||
chr11:46382133-46382384 | Rare:84 | ||||
chr11:46593985-46594121 | Common:1; Rare:32 | ||||
chr11:46617172-46617588 | Common:5; Rare:116 | ||||
chr11:46700553-46700796 | Common:1; Rare:66 | ||||
chr11:46700999-46701077 | Common:1; Rare:30 | ||||
chr11:46846211-46846417 | Common:1; Rare:59 | ||||
chr11:47186408-47186544 | Rare:37 |