Variant report

Variant	rs37527
Chromosome Location	chr5:57571364-57571365
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1035475	1.00[CEU][hapmap]
rs10472035	0.88[CEU][hapmap]
rs10472036	0.88[CEU][hapmap]
rs10513142	0.81[AFR][1000 genomes]
rs13159047	1.00[YRI][hapmap]
rs13168414	1.00[YRI][hapmap]
rs1469090	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs151868	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs152010	1.00[YRI][hapmap]
rs154670	0.89[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs154671	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs154673	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs17709103	1.00[YRI][hapmap]
rs181745	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs1981838	0.88[CEU][hapmap]
rs2052547	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2081087	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2216678	0.84[AFR][1000 genomes]
rs2216679	0.88[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2434584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs245282	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs245285	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs245287	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs245295	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs245296	0.84[AFR][1000 genomes]
rs245493	1.00[YRI][hapmap]
rs246114	0.84[AFR][1000 genomes]
rs27210	0.81[AFR][1000 genomes]
rs27211	0.81[AFR][1000 genomes]
rs27840	0.81[AFR][1000 genomes]
rs2910569	0.88[CEU][hapmap]
rs2910573	1.00[YRI][hapmap]
rs2910577	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2910592	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2910594	0.88[CEU][hapmap]
rs2910600	0.88[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2910601	0.88[CEU][hapmap]
rs2910605	0.88[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2910611	0.88[CEU][hapmap]
rs2964173	0.89[JPT][hapmap]
rs2964184	0.88[CEU][hapmap]
rs2964193	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2964195	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2964200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2964205	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35263833	0.81[AFR][1000 genomes]
rs37484	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs37485	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs37486	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs37487	0.95[ASN][1000 genomes]
rs37488	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs37492	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs37516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs37523	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs37528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37533	0.88[AFR][1000 genomes]
rs37536	1.00[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs40209	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40210	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs41384	0.89[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs42963	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58174847	0.81[AFR][1000 genomes]
rs989579	1.00[YRI][hapmap]

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	esv3489100	chr5:57545689-57669673	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3489101	chr5:57545689-57669673	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2762520	chr5:57557770-57578659	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57567000-57571600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:57568200-57571800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:57570200-57575800	Weak transcription	HMEC	breast
4	chr5:57570200-57577000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:57570400-57574800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:57570400-57575000	Weak transcription	HUVEC	blood vessel
7	chr5:57570400-57575000	Weak transcription	NHEK	skin
8	chr5:57570600-57575000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:57571200-57571400	Enhancers	Primary hematopoietic stem cells	blood

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