Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11132951	0.81[CEU][hapmap]
rs11132952	0.85[CEU][hapmap]
rs12503858	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12642131	0.85[CEU][hapmap]
rs13102637	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs13123441	1.00[CEU][hapmap];0.93[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13124556	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13144240	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1472370	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs1472371	0.81[CEU][hapmap];0.87[CHB][hapmap];0.89[JPT][hapmap]
rs17307651	0.81[CEU][hapmap]
rs180146	0.89[JPT][hapmap]
rs35640087	0.83[EUR][1000 genomes]
rs4476577	0.87[EUR][1000 genomes]
rs4692921	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4695771	0.81[CEU][hapmap]
rs6855645	0.81[CEU][hapmap]
rs6858309	0.80[CEU][hapmap]
rs7658615	0.82[CEU][hapmap]
rs7672525	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs7696315	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]

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	nsv1031592	chr4:173112542-173662991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537359	chr4:173112542-173662991	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv534293	chr4:173121379-173606082	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173493600-173495400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:173494600-173495400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:173494800-173495200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr4:173494800-173495400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr4:173494800-173495400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
6	chr4:173494800-173495400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:173494800-173495400	Enhancers	Adipose Nuclei	Adipose
8	chr4:173494800-173495400	Enhancers	HUVEC	blood vessel
9	chr4:173495000-173495400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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