Variant report

Variant	rs7967956
Chromosome Location	chr12:40265125-40265126
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10747886	0.96[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10747932	0.85[ASN][1000 genomes]
rs10784079	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10784118	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10784208	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10784223	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10784228	0.82[ASN][1000 genomes]
rs10784234	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10877533	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10877733	0.81[JPT][hapmap]
rs10877768	0.83[JPT][hapmap]
rs11173822	0.85[EUR][1000 genomes]
rs11174104	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11174153	0.81[JPT][hapmap]
rs11174238	0.83[JPT][hapmap]
rs11612814	0.81[JPT][hapmap]
rs12813110	0.81[ASN][1000 genomes]
rs4293188	0.92[CHB][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4310675	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4318032	0.82[CEU][hapmap];0.92[CHB][hapmap]
rs4350423	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4357761	0.87[ASN][1000 genomes]
rs4370998	0.85[ASN][1000 genomes]
rs4382970	0.85[ASN][1000 genomes]
rs4388962	0.85[ASN][1000 genomes]
rs4423249	0.82[ASN][1000 genomes]
rs4429129	0.81[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4433640	0.85[CHB][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4473001	0.82[CEU][hapmap];0.93[CHB][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4473002	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4531537	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4539398	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4579982	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4598727	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4604958	0.85[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4638370	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4638371	0.84[CEU][hapmap];0.89[CHB][hapmap];0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4768188	0.88[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4768189	0.92[CHB][hapmap];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6581365	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6581378	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6581403	0.85[CEU][hapmap];0.91[CHB][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6581405	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7133478	0.89[ASN][1000 genomes]
rs7134335	0.89[ASN][1000 genomes]
rs7135701	0.92[CHB][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7294916	0.96[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7295029	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7295344	0.92[CHB][hapmap];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7298896	0.88[JPT][hapmap]
rs7299208	0.81[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7304797	0.89[CEU][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7306234	0.92[CHB][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7308155	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7315452	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7358574	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7958983	0.88[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7959259	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7960098	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7961625	1.00[CHB][hapmap];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7962260	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7963511	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7963645	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7966294	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7968509	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs956066	0.81[JPT][hapmap]
rs9668722	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899025	chr12:40191778-40321846	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv1049214	chr12:40197549-40326495	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv1046428	chr12:40226283-40439843	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv541481	chr12:40226283-40439843	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40199200-40265400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr12:40209200-40268800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr12:40219800-40272600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:40226400-40275000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr12:40232600-40267800	Weak transcription	Liver	Liver
6	chr12:40235200-40269200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr12:40247000-40272000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:40247200-40272800	Weak transcription	Left Ventricle	heart
9	chr12:40248800-40268200	Weak transcription	Fetal Intestine Large	intestine
10	chr12:40253400-40265800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr12:40262600-40280000	Weak transcription	Small Intestine	intestine
12	chr12:40262800-40272600	Weak transcription	Pancreas	Pancrea

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