Variant report

Variant	rs9327012
Chromosome Location	chr5:115922669-115922670
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10045872	0.95[ASN][1000 genomes]
rs10053792	0.96[ASN][1000 genomes]
rs10061055	0.99[ASN][1000 genomes]
rs10062998	0.99[ASN][1000 genomes]
rs10066922	0.96[ASN][1000 genomes]
rs10070276	0.87[ASN][1000 genomes]
rs10073289	0.86[ASN][1000 genomes]
rs10074788	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10075410	0.96[ASN][1000 genomes]
rs10080023	0.96[ASN][1000 genomes]
rs1027742	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs11953558	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12719220	0.95[ASN][1000 genomes]
rs13354122	0.96[ASN][1000 genomes]
rs13355655	0.95[ASN][1000 genomes]
rs13357599	0.94[ASN][1000 genomes]
rs13360587	1.00[ASN][1000 genomes]
rs1345706	0.94[ASN][1000 genomes]
rs1345707	0.94[ASN][1000 genomes]
rs17140120	0.81[CHB][hapmap];1.00[CHD][hapmap];0.86[ASN][1000 genomes]
rs17140171	0.93[ASN][1000 genomes]
rs17140176	0.93[ASN][1000 genomes]
rs1862372	0.94[CHB][hapmap];0.93[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs1862373	0.80[ASN][1000 genomes]
rs2840113	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs28489253	0.93[ASN][1000 genomes]
rs3806914	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs3806915	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs3806916	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs56257700	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs57497884	0.96[ASN][1000 genomes]
rs57557217	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58364462	0.92[ASN][1000 genomes]
rs59351578	1.00[ASN][1000 genomes]
rs6878936	0.96[ASN][1000 genomes]
rs6897765	0.96[ASN][1000 genomes]
rs6898172	0.96[ASN][1000 genomes]
rs73780374	0.85[ASN][1000 genomes]
rs73780375	0.85[ASN][1000 genomes]
rs9327010	0.96[ASN][1000 genomes]
rs9327011	0.96[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	esv2763490	chr5:115918339-116138525	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115912400-115930000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:115913200-115927200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:115920200-115929400	Weak transcription	Pancreas	Pancrea

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