Variant report

Variant	rs11176421
Chromosome Location	chr12:40787679-40787680
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1019709	1.00[CHB][hapmap];0.84[JPT][hapmap];0.95[ASN][1000 genomes]
rs10467146	0.89[JPT][hapmap];0.81[EUR][1000 genomes]
rs10784548	0.89[JPT][hapmap];0.80[EUR][1000 genomes]
rs10784585	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs10784589	0.82[ASN][1000 genomes]
rs10784595	0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs10784596	0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs10878441	0.89[JPT][hapmap];0.80[EUR][1000 genomes]
rs10878507	0.94[ASN][1000 genomes]
rs11176495	0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs12314982	0.93[YRI][hapmap];0.82[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12426362	0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs1365770	0.80[EUR][1000 genomes]
rs1444221	0.81[EUR][1000 genomes]
rs1465528	0.80[EUR][1000 genomes]
rs17466605	0.85[JPT][hapmap];0.80[EUR][1000 genomes]
rs1820544	0.81[ASN][1000 genomes]
rs1820545	0.81[CHB][hapmap];0.85[ASN][1000 genomes]
rs2081700	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2081701	0.95[JPT][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2404840	0.82[CHB][hapmap];0.83[ASN][1000 genomes]
rs2896982	0.95[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3761863	0.89[JPT][hapmap];0.80[EUR][1000 genomes]
rs3886747	0.89[JPT][hapmap];0.80[EUR][1000 genomes]
rs3906483	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4280068	0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4351885	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4767973	0.81[EUR][1000 genomes]
rs4768236	0.89[JPT][hapmap];0.81[EUR][1000 genomes]
rs4768237	0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs5010412	0.81[EUR][1000 genomes]
rs7134408	0.81[JPT][hapmap];0.80[EUR][1000 genomes]
rs7137809	0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs7308560	0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs7310390	0.95[JPT][hapmap];0.96[YRI][hapmap]
rs7954318	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7968048	0.80[EUR][1000 genomes]
rs7968721	0.90[AFR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7972535	0.82[ASN][1000 genomes]
rs7975124	0.95[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs963243	0.85[JPT][hapmap]
rs994798	0.81[JPT][hapmap];0.82[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	nsv832377	chr12:40704881-40855223	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv899032	chr12:40735939-40827479	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv558598	chr12:40742363-40828264	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv1047639	chr12:40774370-40804386	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	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	chr12:40787200-40799200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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