Variant report

Variant	rs71478593
Chromosome Location	chr11:102570333-102570334
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11821641	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11828553	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12272186	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12289076	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17099394	0.86[EUR][1000 genomes]
rs34057617	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34347515	0.86[EUR][1000 genomes]
rs35248432	0.86[EUR][1000 genomes]
rs35594127	0.86[EUR][1000 genomes]
rs35602886	0.86[EUR][1000 genomes]
rs35896366	0.86[EUR][1000 genomes]
rs57646005	0.86[EUR][1000 genomes]
rs73588675	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9704711	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1037454	chr11:102487521-102601233	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541156	chr11:102487521-102601233	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr11:102568800-102572000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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Input of quick search could be:

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

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