Variant report

Variant	rs12711318
Chromosome Location	chr4:160536041-160536042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10004655	0.84[ASN][1000 genomes]
rs10213093	0.80[ASN][1000 genomes]
rs10517703	0.81[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs11100246	0.82[ASN][1000 genomes]
rs11100247	0.82[ASN][1000 genomes]
rs11721796	0.86[ASN][1000 genomes]
rs11730807	0.83[ASN][1000 genomes]
rs11737328	0.81[ASN][1000 genomes]
rs12499316	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12512433	0.82[ASN][1000 genomes]
rs12641814	0.81[ASN][1000 genomes]
rs12641842	0.82[ASN][1000 genomes]
rs12641886	0.82[ASN][1000 genomes]
rs12647153	0.80[EUR][1000 genomes]
rs12647897	0.82[ASN][1000 genomes]
rs12648608	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12648744	0.82[ASN][1000 genomes]
rs13103444	0.82[EUR][1000 genomes]
rs13112184	0.81[EUR][1000 genomes]
rs13138857	0.87[ASN][1000 genomes]
rs13138862	0.88[ASN][1000 genomes]
rs13340212	0.83[ASN][1000 genomes]
rs13340269	0.83[ASN][1000 genomes]
rs1502742	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1566701	0.81[ASN][1000 genomes]
rs1566702	0.81[ASN][1000 genomes]
rs1566703	0.81[ASN][1000 genomes]
rs1566704	0.81[ASN][1000 genomes]
rs1847201	0.82[ASN][1000 genomes]
rs2134423	0.81[ASN][1000 genomes]
rs2134424	0.81[ASN][1000 genomes]
rs2221313	0.90[ASN][1000 genomes]
rs28577259	0.81[ASN][1000 genomes]
rs28713322	0.86[ASN][1000 genomes]
rs2881907	0.82[ASN][1000 genomes]
rs35134080	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35903720	0.81[ASN][1000 genomes]
rs3929449	0.81[ASN][1000 genomes]
rs4303932	0.81[ASN][1000 genomes]
rs4303935	0.81[ASN][1000 genomes]
rs4328868	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4346600	0.81[ASN][1000 genomes]
rs4383572	0.80[ASN][1000 genomes]
rs4499661	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4499662	0.81[ASN][1000 genomes]
rs4536877	0.86[ASN][1000 genomes]
rs4550866	0.81[ASN][1000 genomes]
rs4579071	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4579072	0.80[ASN][1000 genomes]
rs4610292	0.81[ASN][1000 genomes]
rs4613519	0.80[ASN][1000 genomes]
rs4618267	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4691581	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4691582	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4691584	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4691589	0.82[ASN][1000 genomes]
rs4691593	0.80[ASN][1000 genomes]
rs4691594	0.81[ASN][1000 genomes]
rs4691595	0.81[ASN][1000 genomes]
rs4691596	0.81[ASN][1000 genomes]
rs4691597	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5013975	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56162021	0.84[ASN][1000 genomes]
rs62337280	0.81[EUR][1000 genomes]
rs67111572	0.81[ASN][1000 genomes]
rs6826570	0.81[ASN][1000 genomes]
rs6852085	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7655160	0.82[EUR][1000 genomes]
rs7659355	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7675005	0.80[ASN][1000 genomes]
rs7682849	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv881205	chr4:160516090-160628006	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160527400-160536400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:160535800-160536800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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