Variant report

Variant	rs1532728
Chromosome Location	chr14:79495186-79495187
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 136 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:129)

rs_ID	r²[population]
rs10133874	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10135754	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10135769	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10139452	0.83[EUR][1000 genomes]
rs10139460	0.89[CEU][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10141828	0.89[CEU][hapmap]
rs10141996	0.80[EUR][1000 genomes]
rs10142256	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10142652	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10143998	0.82[EUR][1000 genomes]
rs10146180	0.89[CEU][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10146527	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10146542	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10147558	0.89[CEU][hapmap]
rs10147940	0.85[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10150011	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10151590	0.85[CEU][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11159391	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11159392	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11159395	0.89[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap]
rs11625343	0.89[CEU][hapmap]
rs11627661	0.88[CEU][hapmap]
rs11627905	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs11627971	0.93[CEU][hapmap];0.81[EUR][1000 genomes]
rs11849134	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12147468	0.89[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12147527	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12147740	0.89[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12323794	0.89[CEU][hapmap]
rs12431671	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[AMR][1000 genomes]
rs12432817	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12434809	0.89[CEU][hapmap];0.87[CHB][hapmap];0.93[JPT][hapmap]
rs12435865	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12436277	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12586394	0.89[CEU][hapmap]
rs12880287	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12881434	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes]
rs12882464	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12887850	0.89[CEU][hapmap];0.88[CHB][hapmap];0.92[JPT][hapmap]
rs12894123	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes]
rs12895916	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs12897265	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1405474	0.93[CEU][hapmap];0.81[EUR][1000 genomes]
rs1532729	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs154325	0.93[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs1547533	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1547535	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1566675	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17108558	0.87[EUR][1000 genomes]
rs17108575	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs1875595	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1995411	0.89[CEU][hapmap];0.85[AMR][1000 genomes]
rs2035284	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes]
rs2062740	0.89[CEU][hapmap]
rs2062741	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs2062744	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs2062746	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs2088966	0.88[CEU][hapmap]
rs2088967	0.89[CEU][hapmap]
rs2202167	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2202168	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2202171	0.89[CEU][hapmap]
rs2202172	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2202175	0.81[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.83[AMR][1000 genomes]
rs2202179	0.81[AMR][1000 genomes]
rs2202183	0.81[AMR][1000 genomes]
rs2202185	0.93[CEU][hapmap];0.84[EUR][1000 genomes]
rs2221297	0.89[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2370895	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2370900	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2370901	1.00[CHB][hapmap];0.93[JPT][hapmap];0.80[AMR][1000 genomes]
rs2620398	0.85[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap]
rs28831381	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2887887	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs31406	0.80[EUR][1000 genomes]
rs35916059	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4899732	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs4903811	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4903812	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4903813	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4903816	0.89[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes]
rs4903819	0.89[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap]
rs4903820	0.89[CEU][hapmap];0.88[CHB][hapmap];0.92[JPT][hapmap]
rs4903823	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs4903830	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[AMR][1000 genomes]
rs4903833	0.85[CEU][hapmap]
rs61639937	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6574478	0.89[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes]
rs6574480	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6574492	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs6574493	0.89[CEU][hapmap]
rs7142308	0.96[CEU][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7142821	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7149325	0.84[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes]
rs7155818	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7157779	0.89[CEU][hapmap]
rs7161610	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs72687406	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8004582	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes]
rs8005334	0.85[CEU][hapmap]
rs8006615	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8006983	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8007813	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8008393	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8008781	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8009329	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8009383	0.85[CEU][hapmap]
rs8009417	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8010365	0.89[CEU][hapmap];0.89[CHB][hapmap];0.92[JPT][hapmap]
rs8010673	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs8011832	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs8012099	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8013072	0.81[AMR][1000 genomes]
rs8016232	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs8016756	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs8017018	0.88[CEU][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8017027	0.91[EUR][1000 genomes]
rs8018180	0.84[AMR][1000 genomes]
rs8019071	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8020811	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs872483	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs874316	0.90[EUR][1000 genomes]
rs874317	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9323669	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9323670	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9323671	0.89[CEU][hapmap]
rs937648	0.89[CEU][hapmap]
rs9652299	0.90[EUR][1000 genomes]
rs997842	0.89[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917249	chr14:79388181-79574717	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1037112	chr14:79412455-79527656	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1046464	chr14:79478352-79514789	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	lncRNA	n/a	inside rSNPs	diseases
6	nsv1036542	chr14:79478352-79518230	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	lncRNA	n/a	inside rSNPs	diseases
7	nsv948724	chr14:79484233-79614043	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79493600-79495800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:79493800-79495400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr14:79493800-79495600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:79493800-79495600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr14:79494400-79495400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr14:79494600-79495200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:79494600-79495200	Enhancers	NHEK	skin
8	chr14:79494600-79495400	Enhancers	HUVEC	blood vessel
9	chr14:79495000-79495200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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