Variant report

Variant	rs17259910
Chromosome Location	chr2:213334817-213334818
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10497975	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11888697	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11892661	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12987104	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13000748	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13000920	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13015808	0.86[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs13027397	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1505370	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1505371	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1505377	0.85[CEU][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17259208	1.00[YRI][hapmap]
rs17261653	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17262115	0.95[CEU][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17325612	0.89[CEU][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17325821	0.90[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17327185	0.90[CEU][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1921629	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1982717	0.90[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2062929	0.85[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2062931	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34511581	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34947061	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35610945	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56102637	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56387110	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62186285	0.85[EUR][1000 genomes]
rs62186286	0.85[EUR][1000 genomes]
rs62186287	0.85[EUR][1000 genomes]
rs62186292	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62186293	1.00[ASN][1000 genomes]
rs7575120	0.83[EUR][1000 genomes]
rs979452	0.90[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs982075	0.89[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[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	nsv1004573	chr2:213186537-213365252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv875811	chr2:213200920-213347104	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv432024	chr2:213314899-213446726	Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213334000-213335200	Enhancers	Fetal Heart	heart

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