Variant report

Variant	rs2843860
Chromosome Location	chr8:36378197-36378198
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10503990	0.85[EUR][1000 genomes]
rs10503991	0.82[EUR][1000 genomes]
rs10955002	0.85[EUR][1000 genomes]
rs11995775	0.83[EUR][1000 genomes]
rs12675630	0.85[EUR][1000 genomes]
rs16885196	0.85[EUR][1000 genomes]
rs16885201	0.85[EUR][1000 genomes]
rs16885203	0.85[EUR][1000 genomes]
rs2703870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2703871	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2703872	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2843857	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2843858	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2843859	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2843861	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56804036	0.82[EUR][1000 genomes]
rs59625671	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6468367	0.85[EUR][1000 genomes]
rs6468368	0.82[EUR][1000 genomes]
rs6468370	0.81[EUR][1000 genomes]
rs6994820	0.85[EUR][1000 genomes]
rs6996116	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7005989	0.82[EUR][1000 genomes]
rs7010462	0.82[EUR][1000 genomes]
rs73599493	0.85[EUR][1000 genomes]
rs73599494	0.85[EUR][1000 genomes]
rs73599496	0.85[EUR][1000 genomes]
rs73601422	0.81[EUR][1000 genomes]
rs763878	0.85[EUR][1000 genomes]
rs7822796	0.85[EUR][1000 genomes]
rs7830903	0.82[EUR][1000 genomes]
rs7845504	0.85[EUR][1000 genomes]
rs9642714	0.85[EUR][1000 genomes]
rs9642760	0.83[EUR][1000 genomes]
rs9642761	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034989	chr8:36242017-36436244	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1026897	chr8:36252557-36435042	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1023238	chr8:36252557-36530138	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1021042	chr8:36255132-36436244	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	esv2761423	chr8:36255144-36403035	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1015637	chr8:36307431-36439165	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv520391	chr8:36331511-36384831	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv982088	chr8:36374918-36385547	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36376200-36380800	Weak transcription	Placenta Amnion	Placenta Amnion

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