Variant report

Variant	rs13160664
Chromosome Location	chr5:94368609-94368610
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10463164	0.83[ASN][1000 genomes]
rs11135418	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11747168	0.83[ASN][1000 genomes]
rs13155160	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13156286	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13163860	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13181869	0.86[CHB][hapmap]
rs1426098	0.85[YRI][hapmap]
rs1426100	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1593464	0.84[CEU][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs2011547	0.88[ASN][1000 genomes]
rs2114194	0.81[ASN][1000 genomes]
rs2194946	1.00[ASN][1000 genomes]
rs2347478	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4869119	0.91[CHB][hapmap];0.96[JPT][hapmap];0.91[ASN][1000 genomes]
rs4869227	0.95[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs4869228	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[ASN][1000 genomes]
rs4988879	0.82[CHB][hapmap];0.83[JPT][hapmap];0.87[ASN][1000 genomes]
rs6862790	0.82[CHB][hapmap];0.82[JPT][hapmap];0.88[YRI][hapmap];0.86[ASN][1000 genomes]
rs735989	0.87[CHB][hapmap];0.88[YRI][hapmap]
rs7728007	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7729095	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7730096	0.87[CHB][hapmap];0.85[YRI][hapmap];0.82[ASN][1000 genomes]
rs929989	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756469	chr5:94323268-94400017	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94349000-94377800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:94362800-94369600	Enhancers	HUVEC	blood vessel
3	chr5:94364200-94371000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr5:94366400-94369000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:94366400-94371800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr5:94366400-94374200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:94367200-94371600	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr5:94368600-94369400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood

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