Variant report

Variant	rs4756859
Chromosome Location	chr11:16685192-16685193
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs4132853	0.81[EUR][1000 genomes]
rs4256940	0.82[EUR][1000 genomes]
rs4365016	0.84[EUR][1000 genomes]
rs4375406	0.81[EUR][1000 genomes]
rs4456227	0.90[EUR][1000 genomes]
rs4573649	0.81[EUR][1000 genomes]
rs4756853	0.81[EUR][1000 genomes]
rs4757409	0.90[EUR][1000 genomes]
rs4757412	0.90[EUR][1000 genomes]
rs4757418	0.93[EUR][1000 genomes]
rs55684437	0.90[EUR][1000 genomes]
rs55928688	0.90[EUR][1000 genomes]
rs56225716	0.81[EUR][1000 genomes]
rs59872066	0.90[EUR][1000 genomes]
rs66506578	0.90[EUR][1000 genomes]
rs66650309	0.90[EUR][1000 genomes]
rs67055609	0.88[EUR][1000 genomes]
rs67244957	0.90[EUR][1000 genomes]
rs68176835	0.88[EUR][1000 genomes]
rs7115472	0.90[EUR][1000 genomes]
rs7116277	0.90[EUR][1000 genomes]
rs7120735	0.90[EUR][1000 genomes]
rs7122236	0.90[EUR][1000 genomes]
rs7131206	0.83[EUR][1000 genomes]
rs72859412	0.90[EUR][1000 genomes]
rs72859418	0.90[EUR][1000 genomes]
rs72859435	0.90[EUR][1000 genomes]
rs72859451	0.90[EUR][1000 genomes]
rs72859457	0.90[EUR][1000 genomes]
rs72859461	0.86[EUR][1000 genomes]
rs72859475	0.90[EUR][1000 genomes]
rs72859478	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs72859480	0.90[EUR][1000 genomes]
rs72859488	0.90[EUR][1000 genomes]
rs72859492	0.90[EUR][1000 genomes]
rs72861207	0.93[EUR][1000 genomes]
rs72861211	0.93[EUR][1000 genomes]
rs72862543	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72873349	0.81[EUR][1000 genomes]
rs72873376	0.81[EUR][1000 genomes]
rs72873390	0.81[EUR][1000 genomes]
rs72873400	0.84[EUR][1000 genomes]
rs72875203	0.84[EUR][1000 genomes]
rs72875216	0.91[EUR][1000 genomes]
rs72875219	0.90[EUR][1000 genomes]
rs72875220	0.90[EUR][1000 genomes]
rs7925144	0.90[EUR][1000 genomes]
rs7926202	0.90[EUR][1000 genomes]
rs7940952	0.90[EUR][1000 genomes]
rs7944054	0.90[EUR][1000 genomes]
rs9667265	0.90[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	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv897016	chr11:16455794-16691743	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv832076	chr11:16650873-16691808	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3396970	chr11:16658425-16715569	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS	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	chr11:16683800-16686200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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