Variant report

Variant	rs35180056
Chromosome Location	chr10:53839842-53839843
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10762551	0.85[EUR][1000 genomes]
rs10762552	0.85[EUR][1000 genomes]
rs10824011	0.84[EUR][1000 genomes]
rs10824015	0.85[EUR][1000 genomes]
rs10824016	0.85[EUR][1000 genomes]
rs10824017	0.85[EUR][1000 genomes]
rs10824018	0.85[EUR][1000 genomes]
rs10824019	0.83[EUR][1000 genomes]
rs10824020	0.85[EUR][1000 genomes]
rs10824022	0.85[EUR][1000 genomes]
rs10824023	0.85[EUR][1000 genomes]
rs11000668	0.84[EUR][1000 genomes]
rs11000673	0.84[EUR][1000 genomes]
rs11000674	0.84[EUR][1000 genomes]
rs11000675	0.84[EUR][1000 genomes]
rs11000677	0.84[EUR][1000 genomes]
rs11000678	0.84[EUR][1000 genomes]
rs11000679	0.84[EUR][1000 genomes]
rs11000680	0.84[EUR][1000 genomes]
rs11000681	0.84[EUR][1000 genomes]
rs11000684	0.84[EUR][1000 genomes]
rs11000685	0.84[EUR][1000 genomes]
rs11000686	0.83[EUR][1000 genomes]
rs11000687	0.83[EUR][1000 genomes]
rs11000688	0.84[EUR][1000 genomes]
rs11000689	0.84[EUR][1000 genomes]
rs11000690	0.84[EUR][1000 genomes]
rs11000691	0.84[EUR][1000 genomes]
rs11000692	0.84[EUR][1000 genomes]
rs11000693	0.85[EUR][1000 genomes]
rs11000694	0.85[EUR][1000 genomes]
rs11000699	0.85[EUR][1000 genomes]
rs11000705	0.85[EUR][1000 genomes]
rs11000713	0.84[EUR][1000 genomes]
rs12218769	0.85[EUR][1000 genomes]
rs12220039	0.85[EUR][1000 genomes]
rs12769133	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12774871	0.99[ASN][1000 genomes]
rs12782457	0.83[EUR][1000 genomes]
rs1903954	0.85[EUR][1000 genomes]
rs1904025	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1904026	0.84[EUR][1000 genomes]
rs1904028	0.85[EUR][1000 genomes]
rs1904030	0.85[EUR][1000 genomes]
rs1904031	0.85[EUR][1000 genomes]
rs5013005	0.83[EUR][1000 genomes]
rs72803121	0.84[EUR][1000 genomes]
rs72803122	0.84[EUR][1000 genomes]
rs72803123	0.84[EUR][1000 genomes]
rs72803124	0.84[EUR][1000 genomes]
rs7899949	0.82[EUR][1000 genomes]
rs7900083	0.84[EUR][1000 genomes]
rs7900087	0.84[EUR][1000 genomes]
rs7900093	0.84[EUR][1000 genomes]
rs7917109	0.82[EUR][1000 genomes]
rs7920290	0.82[EUR][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	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
3	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
4	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
5	nsv550874	chr10:53816171-53841105	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:53814400-53842800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:53824400-53846200	Weak transcription	Aorta	Aorta
3	chr10:53839800-53852200	Weak transcription	Psoas Muscle	Psoas

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