Variant report

Variant	rs10821316
Chromosome Location	chr9:96971159-96971160
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:96791501..96793535-chr9:96970012..96971868,2	MCF-7	breast:
2	chr9:96927341..96929723-chr9:96969750..96973074,4	K562	blood:
3	chr9:96967187..96969363-chr9:96970249..96972956,2	K562	blood:
4	chr9:96937762..96940255-chr9:96971058..96972798,2	K562	blood:

Variant related genes	Relation type
ENSG00000199072	Chromatin interaction
ENSG00000158079	Chromatin interaction
ENSG00000269929	Chromatin interaction
ENSG00000269946	Chromatin interaction
ENSG00000199165	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10512230	0.85[EUR][1000 genomes]
rs10739971	0.87[EUR][1000 genomes]
rs10739973	0.83[ASN][1000 genomes]
rs10761320	0.85[EUR][1000 genomes]
rs10761323	0.88[EUR][1000 genomes]
rs10761324	0.86[EUR][1000 genomes]
rs10821305	0.85[EUR][1000 genomes]
rs10821306	0.85[EUR][1000 genomes]
rs10821310	0.84[EUR][1000 genomes]
rs10821311	0.88[EUR][1000 genomes]
rs10821317	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10993072	0.85[EUR][1000 genomes]
rs10993073	0.85[EUR][1000 genomes]
rs10993074	0.85[EUR][1000 genomes]
rs10993075	0.81[EUR][1000 genomes]
rs10993095	0.91[AFR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10993096	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10993097	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10993100	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11790972	0.88[EUR][1000 genomes]
rs12004367	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12551019	0.88[EUR][1000 genomes]
rs13293512	0.86[EUR][1000 genomes]
rs2039012	0.88[EUR][1000 genomes]
rs34181781	0.88[EUR][1000 genomes]
rs36030019	0.84[EUR][1000 genomes]
rs7025395	0.86[EUR][1000 genomes]
rs7030004	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7865876	0.86[EUR][1000 genomes]
rs9409706	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9409710	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482457	chr9:96813852-96996170	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	217 gene(s)	inside rSNPs	diseases
2	nsv831655	chr9:96834042-97042009	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	218 gene(s)	inside rSNPs	diseases
3	esv3394266	chr9:96935210-97045514	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	195 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96961200-96973600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:96963200-96971200	Weak transcription	Aorta	Aorta

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