Variant report

Variant	rs2736286
Chromosome Location	chr8:11227104-11227105
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11221017..11222981-chr8:11226248..11228543,2	K562	blood:
2	chr8:11219674..11222977-chr8:11226282..11228003,4	MCF-7	breast:

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10096194	0.92[CEU][hapmap]
rs10098322	0.89[CEU][hapmap]
rs10110557	0.89[CEU][hapmap]
rs1047950	0.82[CEU][hapmap]
rs10503421	0.92[CEU][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11250129	0.81[CEU][hapmap]
rs11777746	0.81[AMR][1000 genomes]
rs11782430	0.81[AMR][1000 genomes]
rs12547100	0.81[AMR][1000 genomes]
rs12549871	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12550129	0.81[AMR][1000 genomes]
rs12681987	0.89[CEU][hapmap];0.80[CHD][hapmap]
rs12682349	0.83[AMR][1000 genomes]
rs13260727	0.81[AMR][1000 genomes]
rs13268126	0.81[AMR][1000 genomes]
rs13274106	0.81[AMR][1000 genomes]
rs1435275	0.83[AMR][1000 genomes]
rs1435277	0.82[CEU][hapmap]
rs17741537	0.92[CEU][hapmap]
rs17797894	0.92[CEU][hapmap]
rs1865521	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2043508	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2043510	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2060456	0.92[CEU][hapmap]
rs2060457	0.89[CEU][hapmap]
rs2060459	0.92[CEU][hapmap]
rs2263511	0.86[AMR][1000 genomes]
rs2263512	0.86[AMR][1000 genomes]
rs2293859	0.89[CEU][hapmap]
rs2293860	0.92[CEU][hapmap]
rs2437152	0.83[AMR][1000 genomes]
rs2572371	0.92[CEU][hapmap];0.88[CHB][hapmap];0.81[CHD][hapmap];0.84[MEX][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2572379	0.83[AMR][1000 genomes]
rs2572380	0.83[AMR][1000 genomes]
rs2572386	0.83[AMR][1000 genomes]
rs2572389	0.83[AMR][1000 genomes]
rs2572391	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2572394	0.83[AMR][1000 genomes]
rs2572395	0.82[AMR][1000 genomes]
rs2572399	0.83[AMR][1000 genomes]
rs2572400	0.83[AMR][1000 genomes]
rs2572440	0.80[AMR][1000 genomes]
rs2572450	0.86[AMR][1000 genomes]
rs2572452	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.98[GIH][hapmap];0.91[JPT][hapmap];0.96[LWK][hapmap];0.84[MEX][hapmap];0.93[MKK][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2736270	0.82[CEU][hapmap]
rs2736280	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.83[JPT][hapmap];0.84[MEX][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2736282	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];0.83[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.82[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2736283	0.92[ASW][hapmap];0.89[CEU][hapmap];0.88[CHB][hapmap];0.98[GIH][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2736285	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2736287	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2736288	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2736290	0.83[AMR][1000 genomes]
rs2736292	0.86[AMR][1000 genomes]
rs2736293	0.83[AMR][1000 genomes]
rs2736294	0.83[AMR][1000 genomes]
rs2736295	0.83[AMR][1000 genomes]
rs2736296	0.83[AMR][1000 genomes]
rs2736297	0.83[AMR][1000 genomes]
rs2736298	0.83[AMR][1000 genomes]
rs2736300	0.83[AMR][1000 genomes]
rs2736302	0.83[AMR][1000 genomes]
rs2736303	0.83[AMR][1000 genomes]
rs2736304	0.82[AMR][1000 genomes]
rs2898272	0.86[AMR][1000 genomes]
rs34964435	0.81[AMR][1000 genomes]
rs35009431	0.81[AMR][1000 genomes]
rs3779891	0.92[CEU][hapmap]
rs4413734	0.92[CEU][hapmap]
rs4448232	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4631424	0.83[AMR][1000 genomes]
rs5029571	0.92[CEU][hapmap]
rs55758514	0.81[AMR][1000 genomes]
rs57629785	0.83[AMR][1000 genomes]
rs6601582	0.85[CEU][hapmap];0.81[AMR][1000 genomes]
rs6601584	0.81[AMR][1000 genomes]
rs6601585	0.86[AMR][1000 genomes]
rs6995404	0.89[CEU][hapmap]
rs7005469	0.92[CEU][hapmap]
rs7016671	0.89[CEU][hapmap]
rs7819395	0.88[CEU][hapmap]
rs7820301	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7821302	0.83[AMR][1000 genomes]
rs7821459	0.83[AMR][1000 genomes]
rs7828263	0.83[AMR][1000 genomes]
rs7834572	0.83[AMR][1000 genomes]
rs7838897	0.89[CEU][hapmap]
rs7839053	0.89[CEU][hapmap]
rs920044	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv831233	chr8:11046854-11234384	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1033312	chr8:11126800-11252170	Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv890354	chr8:11176147-11266131	Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11216000-11227400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr8:11218000-11237600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:11223400-11229000	Weak transcription	Pancreas	Pancrea
4	chr8:11225400-11229800	Weak transcription	K562	blood
5	chr8:11226800-11227600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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