Variant report

Variant	rs7126776
Chromosome Location	chr11:106922701-106922702
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11823197	1.00[AMR][1000 genomes]
rs17106238	1.00[AMR][1000 genomes]
rs17106269	1.00[AMR][1000 genomes]
rs17106297	1.00[AMR][1000 genomes]
rs2883329	1.00[AMR][1000 genomes]
rs55699569	1.00[AMR][1000 genomes]
rs55900807	1.00[AMR][1000 genomes]
rs55911323	1.00[AMR][1000 genomes]
rs56152703	1.00[AMR][1000 genomes]
rs58110753	1.00[AMR][1000 genomes]
rs7932239	1.00[AMR][1000 genomes]
rs7932724	1.00[AMR][1000 genomes]
rs7939110	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531938	chr11:106760733-107156814	Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv527555	chr11:106895032-106971481	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106920600-106923200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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