Variant report

Variant	rs10832841
Chromosome Location	chr11:17701048-17701049
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10741731	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10766418	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10766419	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10766421	0.83[EUR][1000 genomes]
rs10832837	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10832844	0.84[EUR][1000 genomes]
rs11024364	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11024365	0.81[EUR][1000 genomes]
rs11024367	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11024368	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11024375	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12785437	0.83[ASN][1000 genomes]
rs16934571	0.83[ASN][1000 genomes]
rs28683112	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2878806	0.83[ASN][1000 genomes]
rs2878807	0.83[ASN][1000 genomes]
rs3858499	0.83[ASN][1000 genomes]
rs3858501	0.83[ASN][1000 genomes]
rs3858502	0.83[ASN][1000 genomes]
rs3901370	0.83[ASN][1000 genomes]
rs3935159	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4141260	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4141261	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4141262	0.80[EUR][1000 genomes]
rs4756905	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4756907	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4757565	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4757567	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4757568	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4757569	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7395942	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7483014	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9633896	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[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	nsv1040065	chr11:17556031-17753467	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1044126	chr11:17557715-17730646	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv540953	chr11:17557715-17730646	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr11:17699200-17704000	Weak transcription	HSMM	muscle

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