Variant report

Variant	rs73435491
Chromosome Location	chr11:26118099-26118100
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11820372	1.00[AMR][1000 genomes]
rs56695031	1.00[AMR][1000 genomes]
rs59686421	1.00[AMR][1000 genomes]
rs60640095	1.00[AMR][1000 genomes]
rs73437579	1.00[AMR][1000 genomes]
rs73437595	1.00[AMR][1000 genomes]
rs73439603	1.00[AMR][1000 genomes]
rs73439627	1.00[AMR][1000 genomes]
rs73439635	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73439638	1.00[AMR][1000 genomes]
rs73439644	1.00[AMR][1000 genomes]
rs73439645	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26117600-26120000	Enhancers	Fetal Lung	lung
2	chr11:26118000-26118200	Enhancers	Fetal Brain Male	brain
3	chr11:26118000-26118600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte 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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