Variant report

Variant	rs34034708
Chromosome Location	chr4:175605753-175605754
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:175602454..175607122-chr4:175607186..175610908,5	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11939284	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11942827	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1352058	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs25400	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2877826	0.96[ASN][1000 genomes]
rs35117245	0.86[ASN][1000 genomes]
rs35659583	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35817385	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4530609	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4608786	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4627838	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4695784	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61038141	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66471235	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66924837	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs67013670	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6811808	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6811894	0.96[ASN][1000 genomes]
rs6828475	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6847235	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6848286	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72706151	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7438094	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9312557	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[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	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv880584	chr4:175505749-175644689	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:175604400-175605800	Weak transcription	K562	blood

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