Variant report

Variant	rs11000434
Chromosome Location	chr10:53767777-53767778
allele	A/C
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:31)

rs_ID	r²[population]
rs10508950	0.97[ASN][1000 genomes]
rs10762527	1.00[ASN][1000 genomes]
rs10762528	1.00[ASN][1000 genomes]
rs10762538	0.95[ASN][1000 genomes]
rs10823946	1.00[ASN][1000 genomes]
rs10823947	1.00[ASN][1000 genomes]
rs10823948	1.00[ASN][1000 genomes]
rs10823962	1.00[ASN][1000 genomes]
rs10823963	1.00[ASN][1000 genomes]
rs11000432	1.00[ASN][1000 genomes]
rs11000436	1.00[ASN][1000 genomes]
rs11000464	0.97[ASN][1000 genomes]
rs11000472	1.00[ASN][1000 genomes]
rs11000474	1.00[ASN][1000 genomes]
rs11000495	1.00[ASN][1000 genomes]
rs12354901	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12763079	0.95[ASN][1000 genomes]
rs12774183	0.95[ASN][1000 genomes]
rs12776480	1.00[ASN][1000 genomes]
rs1903983	1.00[ASN][1000 genomes]
rs1903985	1.00[ASN][1000 genomes]
rs2246714	1.00[ASN][1000 genomes]
rs2447640	0.97[ASN][1000 genomes]
rs2447641	1.00[ASN][1000 genomes]
rs2454533	1.00[ASN][1000 genomes]
rs2454534	1.00[ASN][1000 genomes]
rs4935025	1.00[ASN][1000 genomes]
rs4935304	1.00[ASN][1000 genomes]
rs4935305	0.95[ASN][1000 genomes]
rs4935306	0.95[ASN][1000 genomes]
rs7895502	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045692	chr10:53301450-54086823	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv519743	chr10:53721665-53773912	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2750961	chr10:53726294-54010594	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv1040754	chr10:53758289-53845925	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:53759200-53768000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:53765800-53770800	Weak transcription	Aorta	Aorta

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