Variant report

Variant	rs4699459
Chromosome Location	chr4:95292702-95292703
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:95266109..95267658-chr4:95291382..95293915,2	K562	blood:
2	chr4:95292208..95293752-chr4:95298604..95300235,2	K562	blood:

Extended variants
information (count: 107 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10020236	0.81[ASN][1000 genomes]
rs10020259	0.98[ASN][1000 genomes]
rs10033087	0.92[ASN][1000 genomes]
rs10033157	0.92[ASN][1000 genomes]
rs10856909	0.83[CEU][hapmap];0.82[CHB][hapmap]
rs11097417	0.83[CEU][hapmap];0.82[CHB][hapmap]
rs11097418	0.82[ASN][1000 genomes]
rs11097419	0.98[ASN][1000 genomes]
rs11097420	1.00[ASN][1000 genomes]
rs11097421	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11097422	0.96[ASN][1000 genomes]
rs11097423	0.98[ASN][1000 genomes]
rs11097426	0.92[ASN][1000 genomes]
rs11721714	0.92[ASN][1000 genomes]
rs11726608	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11726709	0.96[ASN][1000 genomes]
rs11726734	0.95[ASN][1000 genomes]
rs11727030	0.82[CHB][hapmap]
rs11734869	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11734880	0.95[ASN][1000 genomes]
rs11932054	0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11944941	1.00[ASN][1000 genomes]
rs11944992	1.00[ASN][1000 genomes]
rs12507134	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12511686	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12512832	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12646467	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs12646487	0.81[ASN][1000 genomes]
rs12646673	0.81[ASN][1000 genomes]
rs13126976	0.98[ASN][1000 genomes]
rs13133738	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13134502	0.90[ASN][1000 genomes]
rs13146089	0.81[ASN][1000 genomes]
rs13435518	0.98[ASN][1000 genomes]
rs1529339	1.00[ASN][1000 genomes]
rs1593554	0.81[ASN][1000 genomes]
rs1609423	0.98[ASN][1000 genomes]
rs1609424	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17021531	0.81[ASN][1000 genomes]
rs17311521	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17377118	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17565759	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1968332	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1968333	1.00[ASN][1000 genomes]
rs1991316	0.82[CHB][hapmap]
rs2195001	0.81[ASN][1000 genomes]
rs28437833	0.81[ASN][1000 genomes]
rs28458965	0.98[ASN][1000 genomes]
rs28463907	0.98[ASN][1000 genomes]
rs2865353	0.85[CHB][hapmap];0.93[JPT][hapmap]
rs34441565	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3919616	0.81[ASN][1000 genomes]
rs4282187	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs4626213	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4699410	1.00[ASN][1000 genomes]
rs4699411	1.00[ASN][1000 genomes]
rs4699440	0.98[ASN][1000 genomes]
rs4699464	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57939388	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61056400	0.81[ASN][1000 genomes]
rs62320931	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62320932	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62320934	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62321981	0.92[ASN][1000 genomes]
rs6419132	0.82[ASN][1000 genomes]
rs6532480	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6532481	0.81[ASN][1000 genomes]
rs6532482	0.81[ASN][1000 genomes]
rs6532483	0.98[ASN][1000 genomes]
rs6532485	1.00[ASN][1000 genomes]
rs6532486	1.00[ASN][1000 genomes]
rs6532487	1.00[ASN][1000 genomes]
rs6825005	0.81[ASN][1000 genomes]
rs6825431	0.90[ASN][1000 genomes]
rs6826671	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs6826736	0.87[ASN][1000 genomes]
rs6839224	0.81[ASN][1000 genomes]
rs6839950	0.81[ASN][1000 genomes]
rs6840409	0.81[ASN][1000 genomes]
rs6840479	0.81[ASN][1000 genomes]
rs6841656	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6847590	0.92[ASN][1000 genomes]
rs6847767	0.81[ASN][1000 genomes]
rs6847989	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6853674	0.92[ASN][1000 genomes]
rs6856971	0.98[ASN][1000 genomes]
rs6857185	0.98[ASN][1000 genomes]
rs7438414	0.82[CHB][hapmap]
rs7658390	0.98[ASN][1000 genomes]
rs7658431	0.97[ASN][1000 genomes]
rs7658830	1.00[ASN][1000 genomes]
rs7664549	1.00[ASN][1000 genomes]
rs7666873	0.81[ASN][1000 genomes]
rs7670194	0.81[ASN][1000 genomes]
rs7672156	0.85[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7672613	0.98[ASN][1000 genomes]
rs7674215	0.98[ASN][1000 genomes]
rs7675615	0.98[ASN][1000 genomes]
rs7680426	0.98[ASN][1000 genomes]
rs7685514	1.00[ASN][1000 genomes]
rs7691132	0.82[ASN][1000 genomes]
rs7694491	0.86[CHB][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs9997915	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95291800-95293200	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:95291800-95306200	Weak transcription	K562	blood

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