Variant report

Variant	rs12196896
Chromosome Location	chr6:4717873-4717874
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10458178	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11242974	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11242977	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11242978	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11755832	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11759784	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12208133	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12211355	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12214737	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35640627	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35836829	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4960042	0.91[ASN][1000 genomes]
rs6597094	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6597095	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6915353	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6917691	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6931290	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6931832	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6932591	0.95[ASN][1000 genomes]
rs6937790	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6938514	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6941511	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6941562	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7745237	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7748184	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7748335	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7748862	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7762773	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7762927	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7767658	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7767968	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs907841	0.95[ASN][1000 genomes]
rs9328271	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9328272	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9328273	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9328274	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9378409	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9378410	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378411	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9378906	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9378907	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9378908	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378909	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378910	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9392062	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392064	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392626	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392628	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392629	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392630	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9392631	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9392632	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9392634	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9392635	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9405764	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405765	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405766	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405767	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405768	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405769	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9405770	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9405771	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9405772	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9405773	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9405774	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9405776	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9504222	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv528627	chr6:4614058-4731340	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr6:4715600-4719600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:4715800-4726200	Weak transcription	K562	blood

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