Variant report

Variant	rs6843692
Chromosome Location	chr4:125779518-125779519
allele	A/G
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:17)

rs_ID	r²[population]
rs10034348	0.84[AFR][1000 genomes]
rs10518454	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11725383	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11729757	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11729760	0.96[ASN][1000 genomes]
rs11736122	0.85[EUR][1000 genomes]
rs17184412	1.00[CHB][hapmap]
rs2077965	0.83[GIH][hapmap]
rs2086766	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28617665	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59349224	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62323269	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62323271	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62323272	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62323273	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62323299	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7695725	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.96[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	nsv1011752	chr4:125708756-125932456	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1001338	chr4:125708756-126103293	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv830050	chr4:125717858-125888563	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:125776800-125780800	Weak transcription	NHDF-Ad	bronchial
2	chr4:125776800-125783800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:125779000-125783000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:125779400-125781400	Weak transcription	Ovary	ovary

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Input of quick search could be:

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

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