Variant report

Variant	rs11161676
Chromosome Location	chr1:86269261-86269262
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1010058	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.83[ASN][1000 genomes]
rs10747325	1.00[CHB][hapmap]
rs10873722	0.97[ASN][1000 genomes]
rs10873723	0.94[ASN][1000 genomes]
rs10873725	0.92[ASN][1000 genomes]
rs11161677	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11161678	0.97[ASN][1000 genomes]
rs11161682	0.89[ASN][1000 genomes]
rs11161684	0.97[ASN][1000 genomes]
rs11161685	0.97[ASN][1000 genomes]
rs11161686	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11161687	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11579570	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11590890	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12077825	0.87[ASN][1000 genomes]
rs12088004	1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12091583	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12098168	0.87[ASN][1000 genomes]
rs12119620	0.94[ASN][1000 genomes]
rs12128605	1.00[CHB][hapmap];0.86[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12136958	1.00[CHB][hapmap]
rs12727784	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12727916	0.97[ASN][1000 genomes]
rs12735553	0.81[ASN][1000 genomes]
rs12745753	0.81[ASN][1000 genomes]
rs12746325	0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12753056	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12760458	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1325260	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1481199	0.87[ASN][1000 genomes]
rs17404261	1.00[CHB][hapmap]
rs1842579	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2297744	0.83[ASN][1000 genomes]
rs4912437	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4912446	0.84[ASN][1000 genomes]
rs6576790	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6576791	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6576792	0.97[ASN][1000 genomes]
rs6677315	1.00[ASN][1000 genomes]
rs6693669	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6697619	0.87[ASN][1000 genomes]
rs6698139	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6698633	0.97[ASN][1000 genomes]
rs7539262	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv3391173	chr1:86005637-86337469	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv546721	chr1:86226352-86392577	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv999743	chr1:86241246-86364846	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86257200-86274000	Weak transcription	Fetal Lung	lung
2	chr1:86263400-86272200	Weak transcription	GM12878-XiMat	blood
3	chr1:86264600-86272600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:86265800-86272400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:86267400-86273400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:86267600-86271800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:86268000-86270200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr1:86269000-86274000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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