Variant report

Variant	rs6922310
Chromosome Location	chr6:55077184-55077185
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10498801	1.00[CEU][hapmap];0.88[CHB][hapmap];0.88[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10948893	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10948894	1.00[CEU][hapmap];0.88[CHB][hapmap];0.91[CHD][hapmap];0.82[GIH][hapmap];0.88[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12526414	1.00[CEU][hapmap];0.88[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12662510	0.94[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap];0.94[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12663056	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13343017	0.88[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3006854	0.88[CHB][hapmap];0.88[CHD][hapmap];0.88[JPT][hapmap];0.82[TSI][hapmap];0.82[EUR][1000 genomes]
rs3122148	0.91[CHD][hapmap];0.83[JPT][hapmap];0.82[EUR][1000 genomes]
rs3122149	0.94[JPT][hapmap];0.91[MEX][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3122151	0.87[CHB][hapmap];0.88[JPT][hapmap];0.81[EUR][1000 genomes]
rs3122152	0.82[EUR][1000 genomes]
rs3122153	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3134689	0.82[CHB][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes]
rs3134690	0.82[EUR][1000 genomes]
rs3134691	0.82[EUR][1000 genomes]
rs3134692	0.82[EUR][1000 genomes]
rs3134696	0.88[CHB][hapmap];0.88[CHD][hapmap];0.88[JPT][hapmap];0.87[MEX][hapmap];0.85[TSI][hapmap];0.85[EUR][1000 genomes]
rs3134699	0.88[CHB][hapmap];0.91[CHD][hapmap];0.88[JPT][hapmap];0.87[MEX][hapmap];0.82[TSI][hapmap];0.82[EUR][1000 genomes]
rs3134700	0.82[EUR][1000 genomes]
rs3134701	0.88[CHB][hapmap];0.94[JPT][hapmap];0.82[EUR][1000 genomes]
rs3134703	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3134708	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.82[TSI][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4236127	1.00[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55873439	0.81[AMR][1000 genomes]
rs58828550	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59420753	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59682791	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59867521	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs60304167	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6927478	0.82[CHB][hapmap]
rs6937705	1.00[CEU][hapmap];0.88[CHB][hapmap];0.87[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6937878	1.00[CEU][hapmap];0.88[CHB][hapmap];0.88[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6939376	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73434718	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73743300	0.86[AMR][1000 genomes]
rs7775741	0.82[EUR][1000 genomes]
rs7775745	0.88[CHB][hapmap]
rs9367622	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9396060	0.94[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap]
rs9475199	0.83[AMR][1000 genomes]
rs9475200	0.83[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016461	chr6:55038131-55129663	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6922310	GSTA4	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55076200-55077400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:55076600-55077400	Enhancers	HMEC	breast
3	chr6:55076800-55077400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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