Variant report

Variant	rs3775464
Chromosome Location	chr4:90826760-90826761
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10433954	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10433955	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10516850	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10516851	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10516852	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10516853	0.93[CHB][hapmap];0.94[JPT][hapmap]
rs11722543	0.88[ASN][1000 genomes]
rs12640573	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12640925	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12640973	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12641781	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12643823	0.96[ASN][1000 genomes]
rs12644375	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12646270	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs1372511	0.89[ASN][1000 genomes]
rs1372512	0.89[ASN][1000 genomes]
rs1442131	0.99[ASN][1000 genomes]
rs1442132	0.81[CHB][hapmap];0.83[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs16996201	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs17016274	0.88[JPT][hapmap]
rs17016373	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17016396	0.93[CHB][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap]
rs2241884	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3775465	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[ASN][1000 genomes]
rs3775466	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3775467	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3775473	0.85[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs3775474	0.98[ASN][1000 genomes]
rs3775476	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3775477	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs3775478	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs56146644	1.00[ASN][1000 genomes]
rs57925841	0.89[ASN][1000 genomes]
rs58514521	1.00[ASN][1000 genomes]
rs58930449	0.92[ASN][1000 genomes]
rs59559279	0.87[ASN][1000 genomes]
rs60847430	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61160271	0.96[ASN][1000 genomes]
rs61611959	0.90[ASN][1000 genomes]
rs6532197	0.81[CHB][hapmap];0.85[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs6532199	0.89[ASN][1000 genomes]
rs6532200	0.93[CHB][hapmap];0.94[CHD][hapmap];0.87[GIH][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs67212195	0.82[ASN][1000 genomes]
rs6828095	0.89[ASN][1000 genomes]
rs6838943	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6847403	0.89[ASN][1000 genomes]
rs6848022	0.89[ASN][1000 genomes]
rs6857668	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6858182	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72657800	0.99[ASN][1000 genomes]
rs72657801	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72657802	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659403	1.00[ASN][1000 genomes]
rs72659404	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659409	0.98[ASN][1000 genomes]
rs72659413	0.92[ASN][1000 genomes]
rs73831836	0.89[ASN][1000 genomes]
rs73831856	0.95[ASN][1000 genomes]
rs7657014	0.83[ASN][1000 genomes]
rs7666981	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7673735	0.89[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	esv2830400	chr4:90085456-90922432	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv997700	chr4:90791866-90920021	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv830005	chr4:90799398-90963420	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90820000-90827600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:90822200-90827200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:90822800-90830600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr4:90823000-90830400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr4:90825400-90828400	Enhancers	HUVEC	blood vessel
6	chr4:90825600-90826800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr4:90825800-90827000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:90826000-90830400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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