Variant report

Variant	rs1010387
Chromosome Location	chr2:98823261-98823262
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:98822445..98824064-chr2:98827178..98830158,2	K562	blood:

Variant related genes	Relation type
ENSG00000168658	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11684812	1.00[AFR][1000 genomes]
rs11684899	1.00[AFR][1000 genomes]
rs11691306	1.00[AFR][1000 genomes]
rs13402201	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13430738	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.90[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17427608	1.00[AFR][1000 genomes]
rs17427825	1.00[AFR][1000 genomes]
rs17428990	1.00[AFR][1000 genomes]
rs17501094	1.00[AFR][1000 genomes]
rs4564827	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62155312	1.00[AFR][1000 genomes]
rs62155317	1.00[AFR][1000 genomes]
rs62155347	1.00[AFR][1000 genomes]
rs62155355	1.00[AFR][1000 genomes]
rs62155358	1.00[AFR][1000 genomes]
rs62156265	1.00[AFR][1000 genomes]
rs62156266	1.00[AFR][1000 genomes]
rs62156268	1.00[AFR][1000 genomes]
rs62156269	1.00[AFR][1000 genomes]
rs62156346	1.00[AFR][1000 genomes]
rs62156663	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62156681	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62156686	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62156724	1.00[AFR][1000 genomes]
rs62156744	1.00[AFR][1000 genomes]
rs62157892	1.00[AFR][1000 genomes]
rs62157901	1.00[AFR][1000 genomes]
rs62157907	1.00[AFR][1000 genomes]
rs62157908	1.00[AFR][1000 genomes]
rs72817768	0.82[AMR][1000 genomes]
rs72817785	1.00[AFR][1000 genomes]
rs72817792	1.00[AFR][1000 genomes]
rs72817793	1.00[AFR][1000 genomes]
rs72819903	1.00[AFR][1000 genomes]
rs72819919	1.00[AFR][1000 genomes]
rs72819925	1.00[AFR][1000 genomes]
rs9808347	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]

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	nsv521568	chr2:98403683-98826203	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv518056	chr2:98586842-99156296	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1004082	chr2:98792256-98967681	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv535833	chr2:98792256-98967681	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr2:98822200-98823600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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