Variant report

Variant	rs7849811
Chromosome Location	chr9:117468894-117468895
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1077159	0.94[ASN][1000 genomes]
rs11788229	0.88[ASN][1000 genomes]
rs11789008	0.88[ASN][1000 genomes]
rs11789211	1.00[ASN][1000 genomes]
rs11791534	0.88[ASN][1000 genomes]
rs11793258	0.94[ASN][1000 genomes]
rs11794234	0.88[ASN][1000 genomes]
rs11999346	1.00[EUR][1000 genomes]
rs12005760	1.00[EUR][1000 genomes]
rs16930568	1.00[EUR][1000 genomes]
rs16930654	1.00[EUR][1000 genomes]
rs16930926	1.00[ASN][1000 genomes]
rs17237046	0.97[ASN][1000 genomes]
rs17810013	0.94[ASN][1000 genomes]
rs17816047	0.97[ASN][1000 genomes]
rs60476355	1.00[EUR][1000 genomes]
rs61519414	1.00[EUR][1000 genomes]
rs62579741	0.89[ASN][1000 genomes]
rs62579742	0.89[ASN][1000 genomes]
rs62579744	0.97[ASN][1000 genomes]
rs73656160	1.00[EUR][1000 genomes]
rs73656161	1.00[EUR][1000 genomes]
rs73656162	1.00[EUR][1000 genomes]
rs73656191	1.00[EUR][1000 genomes]
rs73656192	1.00[EUR][1000 genomes]
rs73656193	1.00[EUR][1000 genomes]
rs73656194	1.00[EUR][1000 genomes]
rs7850846	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7859926	0.80[AFR][1000 genomes];1.00[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	nsv831694	chr9:117328640-117502785	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv893766	chr9:117385992-117516418	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1042718	chr9:117435306-117488969	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117462200-117471600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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