Variant report

Variant	rs2356661
Chromosome Location	chr8:65136448-65136449
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1010233	0.82[AMR][1000 genomes]
rs1010234	0.82[AMR][1000 genomes]
rs10102832	0.82[AMR][1000 genomes]
rs1011856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1011857	0.82[EUR][1000 genomes]
rs10504374	0.81[ASN][1000 genomes]
rs10808735	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10957303	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11778954	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12680185	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13262660	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13262682	0.82[AMR][1000 genomes]
rs13268763	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1485508	0.82[AMR][1000 genomes]
rs1899051	0.84[AMR][1000 genomes]
rs2356340	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2356341	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2356342	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2356345	0.82[AMR][1000 genomes]
rs2356662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2629620	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2629628	0.83[AMR][1000 genomes]
rs4146360	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4573320	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4588892	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4620321	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7008352	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7464658	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9298080	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs936789	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs936792	0.82[AMR][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	nsv948343	chr8:64804219-65328394	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv534001	chr8:64992196-65798776	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
3	nsv890971	chr8:65028814-65242166	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv1794842	chr8:65123560-65145957	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65134600-65137200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:65134800-65138400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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