Variant report

Variant	rs7751193
Chromosome Location	chr6:164408841-164408842
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10945941	0.82[ASN][1000 genomes]
rs10945942	0.82[ASN][1000 genomes]
rs10945944	0.82[ASN][1000 genomes]
rs10945945	0.82[ASN][1000 genomes]
rs12191111	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12192423	0.81[EUR][1000 genomes]
rs12200803	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16895846	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1756	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34091550	0.87[ASN][1000 genomes]
rs34413611	0.87[ASN][1000 genomes]
rs34561573	0.87[ASN][1000 genomes]
rs34994154	0.85[ASN][1000 genomes]
rs35668088	0.82[ASN][1000 genomes]
rs4499903	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4709030	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4709031	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4709799	0.84[ASN][1000 genomes]
rs4709800	0.84[ASN][1000 genomes]
rs4709802	0.87[ASN][1000 genomes]
rs4709803	0.84[ASN][1000 genomes]
rs4709804	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs473823	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs491901	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs493605	0.83[EUR][1000 genomes]
rs526406	0.83[EUR][1000 genomes]
rs551475	0.81[EUR][1000 genomes]
rs587114	0.83[EUR][1000 genomes]
rs587184	0.83[EUR][1000 genomes]
rs616299	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs617616	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62435541	0.86[ASN][1000 genomes]
rs634032	0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs656371	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs680187	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs717822	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7451221	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9356176	0.87[ASN][1000 genomes]
rs9364711	0.84[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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv830858	chr6:164296054-164455743	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164393800-164413800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:164405600-164409600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:164405600-164412800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr6:164405800-164412400	Weak transcription	Brain Anterior Caudate	brain
5	chr6:164406600-164409000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:164407000-164409600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:164407000-164412400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr6:164407400-164409600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:164407800-164409800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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