Variant report

Variant	rs17099425
Chromosome Location	chr11:102574244-102574245
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11821641	1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[ASN][1000 genomes]
rs11828553	1.00[ASN][1000 genomes]
rs12272186	1.00[ASN][1000 genomes]
rs12289076	1.00[ASN][1000 genomes]
rs1276270	1.00[ASN][1000 genomes]
rs12785370	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12794384	1.00[ASN][1000 genomes]
rs12795467	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs12802760	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12803000	1.00[ASN][1000 genomes]
rs17099394	0.82[CEU][hapmap];0.93[GIH][hapmap];0.82[MEX][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17099427	1.00[ASW][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17099450	0.90[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28478243	1.00[ASN][1000 genomes]
rs28662184	1.00[ASN][1000 genomes]
rs33927742	1.00[ASN][1000 genomes]
rs33982701	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34057617	0.89[EUR][1000 genomes]
rs34347515	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34430514	0.87[AFR][1000 genomes]
rs34472552	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34802753	1.00[ASN][1000 genomes]
rs34832307	0.87[AFR][1000 genomes]
rs35248432	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35594127	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35602886	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35866072	1.00[ASN][1000 genomes]
rs35896366	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs57646005	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73588675	1.00[ASN][1000 genomes]
rs9704711	0.89[EUR][1000 genomes];1.00[ASN][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	chr11:102572600-102579800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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