Variant report

Variant	rs39601
Chromosome Location	chr14:79447225-79447226
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10135271	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10483919	1.00[JPT][hapmap]
rs10483920	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs12436039	0.90[CEU][hapmap];0.91[EUR][1000 genomes]
rs12886900	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12890815	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12895928	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12897049	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs150775	1.00[JPT][hapmap]
rs154326	1.00[JPT][hapmap]
rs1549265	0.80[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs17108418	1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs17757946	1.00[JPT][hapmap]
rs17757966	1.00[JPT][hapmap]
rs17757972	1.00[JPT][hapmap]
rs17757990	0.80[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs17758002	0.80[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs17758014	0.80[CEU][hapmap]
rs17758056	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17835842	1.00[JPT][hapmap]
rs17835893	1.00[JPT][hapmap]
rs17835908	1.00[JPT][hapmap]
rs17835914	1.00[JPT][hapmap]
rs257211	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs31431	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs31444	1.00[JPT][hapmap]
rs31451	1.00[JPT][hapmap]
rs34559943	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71414773	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71414775	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71414776	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs718787	1.00[JPT][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	nsv917249	chr14:79388181-79574717	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1037112	chr14:79412455-79527656	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr14:79447200-79450800	Weak transcription	H9 Cell Line	embryonic stem cell

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