Variant report

Variant	rs12646467
Chromosome Location	chr4:95288819-95288820
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:95281322..95284168-chr4:95287394..95289244,2	K562	blood:
2	chr4:95287113..95289121-chr4:95292704..95294329,2	K562	blood:

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10006191	0.93[ASN][1000 genomes]
rs10020236	0.97[ASN][1000 genomes]
rs10020259	0.82[ASN][1000 genomes]
rs10856909	0.82[CEU][hapmap];0.95[CHB][hapmap];0.86[ASN][1000 genomes]
rs11097417	0.82[CEU][hapmap];0.95[CHB][hapmap];0.86[ASN][1000 genomes]
rs11097418	0.98[ASN][1000 genomes]
rs11097419	0.82[ASN][1000 genomes]
rs11097420	0.84[ASN][1000 genomes]
rs11097421	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11097422	0.80[ASN][1000 genomes]
rs11097423	0.82[ASN][1000 genomes]
rs11726608	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11726709	0.80[ASN][1000 genomes]
rs11727030	0.95[CHB][hapmap];0.84[ASN][1000 genomes]
rs11734869	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11932054	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11944941	0.84[ASN][1000 genomes]
rs11944992	0.84[ASN][1000 genomes]
rs12507134	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12511686	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12512832	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12646487	0.97[ASN][1000 genomes]
rs12646673	0.97[ASN][1000 genomes]
rs13126976	0.82[ASN][1000 genomes]
rs13133738	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13146089	0.97[ASN][1000 genomes]
rs13435518	0.82[ASN][1000 genomes]
rs1344612	0.86[ASN][1000 genomes]
rs1529339	0.84[ASN][1000 genomes]
rs1593554	0.97[ASN][1000 genomes]
rs1609423	0.82[ASN][1000 genomes]
rs1609424	0.84[EUR][1000 genomes]
rs17021507	0.89[ASN][1000 genomes]
rs17021531	0.97[ASN][1000 genomes]
rs17311008	0.91[ASN][1000 genomes]
rs17311521	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17377118	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17565759	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1965049	0.85[ASN][1000 genomes]
rs1965696	0.91[ASN][1000 genomes]
rs1968332	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1968333	0.84[ASN][1000 genomes]
rs1991316	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs2195001	0.97[ASN][1000 genomes]
rs28408371	0.89[ASN][1000 genomes]
rs28437833	0.97[ASN][1000 genomes]
rs28458965	0.82[ASN][1000 genomes]
rs28463907	0.82[ASN][1000 genomes]
rs2865353	0.95[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs34181160	0.91[ASN][1000 genomes]
rs34441565	0.92[EUR][1000 genomes]
rs3919616	0.97[ASN][1000 genomes]
rs4282187	0.95[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs4626213	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4699410	0.84[ASN][1000 genomes]
rs4699411	0.84[ASN][1000 genomes]
rs4699440	0.82[ASN][1000 genomes]
rs4699459	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4699464	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57939388	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61056400	0.97[ASN][1000 genomes]
rs62320931	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62320932	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62320934	0.89[EUR][1000 genomes]
rs6419132	0.98[ASN][1000 genomes]
rs6532480	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6532481	0.97[ASN][1000 genomes]
rs6532482	0.97[ASN][1000 genomes]
rs6532483	0.82[ASN][1000 genomes]
rs6532485	0.84[ASN][1000 genomes]
rs6532486	0.84[ASN][1000 genomes]
rs6532487	0.84[ASN][1000 genomes]
rs6825005	0.97[ASN][1000 genomes]
rs6826671	0.95[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs6839224	0.97[ASN][1000 genomes]
rs6839950	0.97[ASN][1000 genomes]
rs6840409	0.97[ASN][1000 genomes]
rs6840479	0.96[ASN][1000 genomes]
rs6841656	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6847767	0.97[ASN][1000 genomes]
rs6847989	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6856971	0.82[ASN][1000 genomes]
rs6857185	0.82[ASN][1000 genomes]
rs7438414	0.95[CHB][hapmap];0.84[ASN][1000 genomes]
rs7657805	0.89[ASN][1000 genomes]
rs7658390	0.82[ASN][1000 genomes]
rs7658431	0.81[ASN][1000 genomes]
rs7658830	0.84[ASN][1000 genomes]
rs7664549	0.84[ASN][1000 genomes]
rs7666873	0.97[ASN][1000 genomes]
rs7670194	0.97[ASN][1000 genomes]
rs7672156	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7672464	0.85[ASN][1000 genomes]
rs7672527	0.86[ASN][1000 genomes]
rs7672613	0.82[ASN][1000 genomes]
rs7672999	0.81[ASN][1000 genomes]
rs7674215	0.82[ASN][1000 genomes]
rs7675615	0.82[ASN][1000 genomes]
rs7680426	0.82[ASN][1000 genomes]
rs7685514	0.84[ASN][1000 genomes]
rs7691132	0.98[ASN][1000 genomes]
rs7694491	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9997915	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993495	chr4:94992315-95482578	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv594901	chr4:95254730-95493246	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1003743	chr4:95255957-95469831	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv519228	chr4:95277311-95292702	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv964074	chr4:95286219-95292123	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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