Variant report

Variant	rs62320934
Chromosome Location	chr4:95307175-95307176
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10020259	0.87[ASN][1000 genomes]
rs10033087	0.80[ASN][1000 genomes]
rs10033157	0.80[ASN][1000 genomes]
rs11097419	0.83[ASN][1000 genomes]
rs11097420	0.85[ASN][1000 genomes]
rs11097421	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11097422	0.85[ASN][1000 genomes]
rs11097423	0.87[ASN][1000 genomes]
rs11097426	0.80[ASN][1000 genomes]
rs11721714	0.80[ASN][1000 genomes]
rs11726608	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11726709	0.85[ASN][1000 genomes]
rs11726734	0.87[ASN][1000 genomes]
rs11734869	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11734880	0.87[ASN][1000 genomes]
rs11944941	0.85[ASN][1000 genomes]
rs11944992	0.85[ASN][1000 genomes]
rs12507134	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12511686	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12512832	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13126976	0.87[ASN][1000 genomes]
rs13133738	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13134502	0.89[ASN][1000 genomes]
rs13435518	0.87[ASN][1000 genomes]
rs1529339	0.85[ASN][1000 genomes]
rs1609423	0.83[ASN][1000 genomes]
rs17311521	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17377118	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17565759	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1968332	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1968333	0.85[ASN][1000 genomes]
rs28458965	0.87[ASN][1000 genomes]
rs28463907	0.87[ASN][1000 genomes]
rs34441565	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4626213	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4699410	0.85[ASN][1000 genomes]
rs4699411	0.85[ASN][1000 genomes]
rs4699440	0.87[ASN][1000 genomes]
rs4699459	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4699464	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57939388	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62320931	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62320932	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62321981	0.80[ASN][1000 genomes]
rs6532483	0.83[ASN][1000 genomes]
rs6532485	0.85[ASN][1000 genomes]
rs6532486	0.85[ASN][1000 genomes]
rs6532487	0.85[ASN][1000 genomes]
rs6841656	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6847590	0.80[ASN][1000 genomes]
rs6853674	0.80[ASN][1000 genomes]
rs6856971	0.83[ASN][1000 genomes]
rs6857185	0.83[ASN][1000 genomes]
rs7658390	0.87[ASN][1000 genomes]
rs7658431	0.86[ASN][1000 genomes]
rs7658830	0.85[ASN][1000 genomes]
rs7664549	0.85[ASN][1000 genomes]
rs7672613	0.83[ASN][1000 genomes]
rs7674215	0.83[ASN][1000 genomes]
rs7675615	0.83[ASN][1000 genomes]
rs7680426	0.83[ASN][1000 genomes]
rs7685514	0.85[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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95305200-95308000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr4:95306000-95307800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:95307000-95309600	Weak transcription	K562	blood

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