Variant report

Variant	rs2066076
Chromosome Location	chr6:132854027-132854028
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11758170	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12195306	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12209085	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12209100	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12210154	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17061384	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2066075	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2066077	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2153171	0.90[ASN][1000 genomes]
rs2153178	0.86[CHB][hapmap];0.85[JPT][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2840835	0.80[JPT][hapmap]
rs58924219	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6569807	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6918805	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7743835	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7763434	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9483478	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9493355	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9493360	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9493361	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9493362	0.88[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9493363	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9493364	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9493365	0.91[EUR][1000 genomes]
rs9493366	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9493367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][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	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 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	chr6:132851800-132854800	Weak transcription	HepG2	liver
2	chr6:132851800-132855800	Weak transcription	Psoas Muscle	Psoas

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