Variant report

Variant	rs10847751
Chromosome Location	chr12:123291742-123291743
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs1026395	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1037593	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10773599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10773627	0.81[YRI][hapmap]
rs10847742	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10847749	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10847775	0.90[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10847910	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10848148	1.00[JPT][hapmap]
rs11060142	0.80[AFR][1000 genomes]
rs11060152	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11060932	1.00[JPT][hapmap]
rs11060999	1.00[JPT][hapmap]
rs11503063	0.86[AMR][1000 genomes]
rs12311043	1.00[JPT][hapmap]
rs12367291	0.80[AFR][1000 genomes]
rs12369710	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1260121	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs12811036	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12824418	0.81[AFR][1000 genomes]
rs1671681	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs1671682	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs1671683	0.95[YRI][hapmap];0.83[AFR][1000 genomes]
rs1671684	1.00[JPT][hapmap]
rs1671687	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1696316	0.83[AFR][1000 genomes]
rs1696321	0.81[YRI][hapmap]
rs1696322	0.93[YRI][hapmap]
rs1696325	1.00[YRI][hapmap]
rs1696355	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs1798560	0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs1798561	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs1798563	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs1798565	0.81[AFR][1000 genomes]
rs1798569	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs1975761	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs2061099	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2343107	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2456151	0.81[AFR][1000 genomes]
rs2649895	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs2649896	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs2649899	0.82[AFR][1000 genomes]
rs2649900	0.87[EUR][1000 genomes]
rs2649903	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs2649914	0.81[EUR][1000 genomes]
rs2656812	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs2656814	0.83[AFR][1000 genomes]
rs3844369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3852535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4038070	0.97[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4038080	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4038081	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4307760	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4424710	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4426165	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4759353	1.00[JPT][hapmap]
rs4759354	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4759355	0.81[YRI][hapmap]
rs4759384	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4759389	0.82[YRI][hapmap]
rs4759391	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4759438	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6489241	1.00[CEU][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs651683	1.00[JPT][hapmap]
rs7138257	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7298176	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7305256	0.86[EUR][1000 genomes]
rs7306948	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7485652	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7487095	0.90[EUR][1000 genomes]
rs7957643	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7958155	1.00[JPT][hapmap]
rs7960548	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs839354	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs839356	0.81[EUR][1000 genomes]
rs839362	0.80[EUR][1000 genomes]
rs897386	0.82[CEU][hapmap]
rs897388	1.00[JPT][hapmap]
rs897391	0.81[YRI][hapmap]
rs897393	0.81[YRI][hapmap]
rs921808	0.81[YRI][hapmap]
rs967281	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9788154	0.89[AFR][1000 genomes]
rs9795629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899571	chr12:123215734-123363562	Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	esv3388790	chr12:123275902-123655103	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123259400-123310600	Weak transcription	HSMMtube	muscle
2	chr12:123259800-123310600	Weak transcription	Brain Substantia Nigra	brain
3	chr12:123260000-123303600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr12:123265600-123303600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:123266000-123303800	Weak transcription	Brain Hippocampus Middle	brain
6	chr12:123278600-123305600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr12:123284400-123297400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:123284800-123293400	Weak transcription	Primary B cells from cord blood	blood
9	chr12:123284800-123297600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:123284800-123297600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:123286600-123303600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr12:123289200-123303800	Weak transcription	Brain Anterior Caudate	brain
13	chr12:123290600-123310400	Weak transcription	Aorta	Aorta
14	chr12:123290800-123291800	Strong transcription	Skeletal Muscle Female	skeletal muscle
15	chr12:123291600-123292600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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