Variant report

Variant	rs7684879
Chromosome Location	chr4:76963251-76963252
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:76961498-76963733	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:76956748..76960411-chr4:76960413..76963338,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM47E-1	chr4:76963127-76963257	l_2670_chr4:76963126-76965818_testes

Variant related genes	Relation type
CXCL11	TF binding region
ENSG00000225846	Chromatin interaction
ENSG00000169248	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10019066	0.82[ASN][1000 genomes]
rs10025961	0.82[ASN][1000 genomes]
rs10030471	0.82[ASN][1000 genomes]
rs10433952	0.82[ASN][1000 genomes]
rs1050176	0.82[ASN][1000 genomes]
rs12499668	0.82[ASN][1000 genomes]
rs12500200	0.82[ASN][1000 genomes]
rs12510239	0.82[ASN][1000 genomes]
rs12511357	0.82[ASN][1000 genomes]
rs12511359	0.82[ASN][1000 genomes]
rs13106039	0.82[ASN][1000 genomes]
rs28484974	0.82[ASN][1000 genomes]
rs28601861	0.82[ASN][1000 genomes]
rs28647509	0.82[ASN][1000 genomes]
rs2869461	0.82[ASN][1000 genomes]
rs35353995	0.82[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs3733236	0.82[ASN][1000 genomes]
rs4404571	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4621456	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55813915	0.82[ASN][1000 genomes]
rs55964684	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs56039229	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs56054611	0.82[ASN][1000 genomes]
rs56316945	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs60282049	0.82[ASN][1000 genomes]
rs60431104	0.82[ASN][1000 genomes]
rs6532084	0.82[ASN][1000 genomes]
rs6532167	0.82[ASN][1000 genomes]
rs6532168	0.82[ASN][1000 genomes]
rs6532169	0.82[ASN][1000 genomes]
rs6532170	0.82[ASN][1000 genomes]
rs67194908	0.82[ASN][1000 genomes]
rs67308118	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs67413521	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67687266	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6857358	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6857378	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7666094	0.82[ASN][1000 genomes]
rs7670156	0.82[ASN][1000 genomes]
rs7671170	0.84[ASN][1000 genomes]
rs7671209	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7676234	0.84[ASN][1000 genomes]
rs7679689	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7685390	0.82[ASN][1000 genomes]
rs7692605	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7693117	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9990658	0.82[ASN][1000 genomes]
rs9998233	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3353539	chr4:76530136-76993859	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv529613	chr4:76654941-77081576	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats 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	38 gene(s)	inside rSNPs	diseases
3	nsv1004627	chr4:76793910-76999584	Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	esv19222	chr4:76948569-76977780	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv1802071	chr4:76948817-76972594	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv594691	chr4:76961802-76972594	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv1810835	chr4:76961802-76974351	Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:76958200-76972600	Weak transcription	Right Atrium	heart
2	chr4:76963200-76963800	Enhancers	HUVEC	blood vessel

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