Variant report

Variant	rs6980392
Chromosome Location	chr7:11661051-11661052
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10236115	0.85[ASN][1000 genomes]
rs10486145	0.81[ASN][1000 genomes]
rs10486146	0.90[ASN][1000 genomes]
rs10486147	0.86[AFR][1000 genomes]
rs16877006	0.83[ASN][1000 genomes]
rs17164940	0.87[ASN][1000 genomes]
rs17164942	0.86[ASN][1000 genomes]
rs17164943	0.85[ASN][1000 genomes]
rs17164945	0.86[ASN][1000 genomes]
rs17164946	0.85[ASN][1000 genomes]
rs17164958	0.85[ASN][1000 genomes]
rs17164960	0.85[ASN][1000 genomes]
rs17519435	0.84[ASN][1000 genomes]
rs17519442	0.84[ASN][1000 genomes]
rs3846987	0.85[AFR][1000 genomes]
rs3846988	0.85[AFR][1000 genomes]
rs4324838	0.81[ASN][1000 genomes]
rs4530931	0.99[ASN][1000 genomes]
rs59757579	0.80[ASN][1000 genomes]
rs6460830	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6950617	0.88[ASN][1000 genomes]
rs6977236	0.83[ASN][1000 genomes]
rs6980266	0.99[ASN][1000 genomes]
rs6980366	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9638674	1.00[CEU][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[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	nsv1028326	chr7:11221209-11754436	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv538733	chr7:11221209-11754436	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1023665	chr7:11457493-11773517	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv887606	chr7:11473561-11771288	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11653800-11665000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr7:11656800-11664800	Weak transcription	HUVEC	blood vessel
3	chr7:11660800-11664800	Weak transcription	Hela-S3	cervix
4	chr7:11660800-11665200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr7:11660800-11665400	Weak transcription	Adipose Nuclei	Adipose
6	chr7:11660800-11681400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:11661000-11661200	Flanking Active TSS	Liver	Liver
8	chr7:11661000-11661400	Weak transcription	A549	lung
9	chr7:11661000-11665000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:11661000-11665400	Weak transcription	Brain Hippocampus Middle	brain

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