Variant report

Variant	rs34327710
Chromosome Location	chr8:85824304-85824305
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10046686	0.87[ASN][1000 genomes]
rs10081441	0.84[ASN][1000 genomes]
rs10088722	0.84[ASN][1000 genomes]
rs10091232	0.83[ASN][1000 genomes]
rs10091245	0.91[ASN][1000 genomes]
rs10094238	0.87[ASN][1000 genomes]
rs10094828	0.86[ASN][1000 genomes]
rs10095636	0.91[ASN][1000 genomes]
rs10095682	0.91[ASN][1000 genomes]
rs10099017	0.91[ASN][1000 genomes]
rs10100687	0.85[ASN][1000 genomes]
rs10100806	0.85[ASN][1000 genomes]
rs10104630	0.84[ASN][1000 genomes]
rs10104687	0.84[ASN][1000 genomes]
rs10105658	0.87[ASN][1000 genomes]
rs10109018	0.84[ASN][1000 genomes]
rs10110570	0.88[ASN][1000 genomes]
rs10110879	0.89[ASN][1000 genomes]
rs1025232	0.87[ASN][1000 genomes]
rs10958229	0.87[ASN][1000 genomes]
rs10958230	0.84[ASN][1000 genomes]
rs10958232	0.86[ASN][1000 genomes]
rs10958233	0.83[ASN][1000 genomes]
rs11775584	0.87[ASN][1000 genomes]
rs12542468	0.84[ASN][1000 genomes]
rs12604	0.84[ASN][1000 genomes]
rs12675186	0.82[ASN][1000 genomes]
rs13267859	0.87[ASN][1000 genomes]
rs13273360	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1365668	0.88[ASN][1000 genomes]
rs1365677	0.91[ASN][1000 genomes]
rs1365678	0.91[ASN][1000 genomes]
rs1404365	0.84[ASN][1000 genomes]
rs1524642	0.85[ASN][1000 genomes]
rs17811680	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1851973	0.85[ASN][1000 genomes]
rs1946400	0.88[ASN][1000 genomes]
rs1991347	0.87[ASN][1000 genomes]
rs1991348	0.87[ASN][1000 genomes]
rs1991349	0.87[ASN][1000 genomes]
rs1991350	0.86[ASN][1000 genomes]
rs1991351	0.87[ASN][1000 genomes]
rs1991352	0.87[ASN][1000 genomes]
rs2059678	0.84[ASN][1000 genomes]
rs2059679	0.83[ASN][1000 genomes]
rs2059680	0.87[ASN][1000 genomes]
rs2081673	0.86[ASN][1000 genomes]
rs2140688	0.84[ASN][1000 genomes]
rs2712	0.87[ASN][1000 genomes]
rs28592585	0.87[ASN][1000 genomes]
rs35382421	0.91[ASN][1000 genomes]
rs3900098	0.87[ASN][1000 genomes]
rs3937521	0.87[ASN][1000 genomes]
rs3942601	0.85[ASN][1000 genomes]
rs4740035	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6990756	0.87[ASN][1000 genomes]
rs7003643	0.86[ASN][1000 genomes]
rs7008839	0.87[ASN][1000 genomes]
rs7010343	0.91[ASN][1000 genomes]
rs7832097	0.84[ASN][1000 genomes]
rs7838564	0.87[ASN][1000 genomes]
rs7838940	0.91[ASN][1000 genomes]
rs9298433	0.84[ASN][1000 genomes]
rs9650296	0.86[ASN][1000 genomes]
rs965734	0.86[ASN][1000 genomes]
rs9692810	0.84[ASN][1000 genomes]
rs9692962	0.84[ASN][1000 genomes]
rs9693371	0.84[ASN][1000 genomes]
rs987477	0.87[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	esv3481417	chr8:85279453-86145229	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv3481418	chr8:85279453-86145229	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv427823	chr8:85538522-86009068	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv891118	chr8:85749529-85827179	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv891119	chr8:85749529-85832893	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv891120	chr8:85749529-85890857	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv891121	chr8:85772129-85827179	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:85822600-85841400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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