Variant report

Variant	rs587114
Chromosome Location	chr6:164414940-164414941
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1005541	0.80[EUR][1000 genomes]
rs10428875	0.80[EUR][1000 genomes]
rs10484512	0.88[EUR][1000 genomes]
rs10484513	0.88[EUR][1000 genomes]
rs10484514	0.87[EUR][1000 genomes]
rs10484515	0.87[EUR][1000 genomes]
rs10945939	0.87[EUR][1000 genomes]
rs10945940	0.88[EUR][1000 genomes]
rs10945941	0.87[EUR][1000 genomes]
rs10945942	0.87[EUR][1000 genomes]
rs10945944	0.87[EUR][1000 genomes]
rs10945945	0.87[EUR][1000 genomes]
rs12192423	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12200803	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12209088	0.83[EUR][1000 genomes]
rs12209089	0.84[EUR][1000 genomes]
rs12215299	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13193552	0.86[EUR][1000 genomes]
rs1545107	0.88[EUR][1000 genomes]
rs205983	0.80[EUR][1000 genomes]
rs206005	0.81[EUR][1000 genomes]
rs2064791	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34021940	0.87[EUR][1000 genomes]
rs34091550	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34413611	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34561573	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34727935	0.87[EUR][1000 genomes]
rs34994154	0.86[EUR][1000 genomes]
rs35668088	0.87[EUR][1000 genomes]
rs4304140	0.86[EUR][1000 genomes]
rs4709799	0.88[EUR][1000 genomes]
rs4709800	0.88[EUR][1000 genomes]
rs4709802	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4709803	0.81[EUR][1000 genomes]
rs473823	0.81[ASN][1000 genomes]
rs493605	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs526406	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs587184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs616299	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs617616	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62435513	0.87[EUR][1000 genomes]
rs62435541	0.89[EUR][1000 genomes]
rs634032	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs680187	0.91[ASN][1000 genomes]
rs680946	0.82[EUR][1000 genomes]
rs735858	0.81[EUR][1000 genomes]
rs7751193	0.83[EUR][1000 genomes]
rs9356176	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9364711	0.91[EUR][1000 genomes]
rs9365634	0.82[EUR][1000 genomes]
rs942009	0.80[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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv830858	chr6:164296054-164455743	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 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	chr6:164412600-164417600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:164414200-164420600	Weak transcription	Brain Anterior Caudate	brain

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