Variant report

Variant	rs4697250
Chromosome Location	chr4:21940697-21940698
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1015950	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1022247	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs10516406	0.96[ASN][1000 genomes]
rs11728026	0.84[ASN][1000 genomes]
rs12502633	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs12509508	0.99[ASN][1000 genomes]
rs13118537	0.96[ASN][1000 genomes]
rs13132720	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13132737	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1849542	0.81[ASN][1000 genomes]
rs1996131	1.00[ASW][hapmap];0.81[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.84[JPT][hapmap];0.92[MEX][hapmap];0.90[TSI][hapmap]
rs2323162	0.81[CEU][hapmap]
rs35494764	1.00[ASN][1000 genomes]
rs4697248	0.92[CEU][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[TSI][hapmap]
rs6820764	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs6831938	0.92[CEU][hapmap];0.80[CHB][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.93[TSI][hapmap]

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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2757924	chr4:21873204-21980559	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv2759231	chr4:21873204-21980559	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428440	chr4:21873204-21980559	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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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