Variant report

Variant	rs11757992
Chromosome Location	chr6:64720214-64720215
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1038316	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1038317	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10944281	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10944299	0.82[EUR][1000 genomes]
rs11759618	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12190415	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12205397	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35431369	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4530841	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4563699	0.83[EUR][1000 genomes]
rs4710458	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs60945987	0.86[ASN][1000 genomes]
rs62415275	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66502009	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6902200	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6909613	0.82[EUR][1000 genomes]
rs6930818	0.81[EUR][1000 genomes]
rs6936438	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs716618	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs727347	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7739137	0.93[EUR][1000 genomes]
rs7749459	0.82[EUR][1000 genomes]
rs7757884	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7760226	0.93[EUR][1000 genomes]
rs7761892	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9342097	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9344655	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9344659	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9344688	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9351111	0.92[EUR][1000 genomes]
rs9351119	0.82[EUR][1000 genomes]
rs9353436	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9353437	0.82[EUR][1000 genomes]
rs9353439	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9353440	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9353441	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9362371	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9362372	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9362375	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9362406	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9444417	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9450605	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs967075	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020226	chr6:64582008-64793525	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv538271	chr6:64582008-64793525	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv603376	chr6:64589465-64771342	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1026162	chr6:64639580-65470828	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv538272	chr6:64639580-65470828	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64720000-64722000	Weak transcription	Fetal Heart	heart
2	chr6:64720200-64720400	Enhancers	Placenta Amnion	Placenta Amnion
3	chr6:64720200-64721600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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