Variant report

Variant	rs1503435
Chromosome Location	chr3:87908816-87908817
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1021845	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158019	1.00[ASN][1000 genomes]
rs1393921	0.81[AFR][1000 genomes]
rs1489775	1.00[ASN][1000 genomes]
rs1503431	1.00[ASN][1000 genomes]
rs1602153	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1812620	1.00[ASN][1000 genomes]
rs1844432	1.00[ASN][1000 genomes]
rs1844433	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897237	1.00[ASN][1000 genomes]
rs1910400	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2130347	1.00[ASN][1000 genomes]
rs2130349	1.00[ASN][1000 genomes]
rs2343772	1.00[EUR][1000 genomes]
rs28690491	1.00[ASN][1000 genomes]
rs2919237	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2919239	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2919245	1.00[ASN][1000 genomes]
rs2919246	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2919247	1.00[ASN][1000 genomes]
rs2919250	1.00[ASN][1000 genomes]
rs2919256	1.00[ASN][1000 genomes]
rs2919257	1.00[ASN][1000 genomes]
rs2919259	1.00[ASN][1000 genomes]
rs2932266	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2932267	1.00[ASN][1000 genomes]
rs2932269	1.00[ASN][1000 genomes]
rs2932271	1.00[ASN][1000 genomes]
rs2932287	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2932297	1.00[ASN][1000 genomes]
rs2932299	0.81[AFR][1000 genomes]
rs2932308	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2938276	0.81[AFR][1000 genomes]
rs2938281	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59395828	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6774364	1.00[ASN][1000 genomes]
rs6777373	1.00[ASN][1000 genomes]
rs6787171	1.00[ASN][1000 genomes]
rs6790616	1.00[ASN][1000 genomes]
rs6796732	1.00[ASN][1000 genomes]
rs6807498	1.00[ASN][1000 genomes]
rs72911631	1.00[ASN][1000 genomes]
rs7641305	1.00[ASN][1000 genomes]
rs923478	0.91[AFR][1000 genomes]
rs9816019	1.00[ASN][1000 genomes]
rs9854145	1.00[ASN][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	nsv590918	chr3:87323334-87910931	Enhancers Bivalent Enhancer Strong transcription Weak 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	8 gene(s)	inside rSNPs	diseases
2	nsv834756	chr3:87763793-87938179	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1009981	chr3:87821573-88003956	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv536634	chr3:87821573-88003956	Bivalent/Poised TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv460757	chr3:87863280-87949733	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv590919	chr3:87863280-87949733	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv834758	chr3:87867363-88014975	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:87867800-87912800	Weak transcription	K562	blood
2	chr3:87904600-87909600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:87906000-87909400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr3:87907600-87909600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr3:87908000-87909000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr3:87908600-87909000	Enhancers	Spleen	Spleen
7	chr3:87908600-87909000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr3:87908800-87909000	Enhancers	A549	lung
9	chr3:87908800-87910200	Genic enhancers	Primary hematopoietic stem cells	blood
10	chr3:87908800-87910200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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