Variant report

Variant	rs73141263
Chromosome Location	chr3:87999098-87999099
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12106679	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12487603	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12490381	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12491305	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12491719	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12493624	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12493756	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12493835	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2068947	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2163422	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55780392	0.87[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs55789120	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55915802	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55960285	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55968109	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56063464	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56064296	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56126309	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56215818	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56231132	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56274317	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56320121	0.84[ASN][1000 genomes]
rs56368064	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56381224	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56386318	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6765538	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6776844	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73141236	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73141241	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73141278	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73147264	0.84[ASN][1000 genomes]
rs73147265	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv1007981	chr3:87949316-88004036	Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv527929	chr3:87949733-88003812	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv877146	chr3:87983962-88159835	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 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	chr3:87995000-88002400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:87995600-88011000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:87997800-87999600	Enhancers	Primary B cells from peripheral blood	blood
4	chr3:87998400-87999200	Weak transcription	Fetal Kidney	kidney
5	chr3:87998600-87999200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:87998600-87999200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:87998800-87999400	Active TSS	GM12878-XiMat	blood
8	chr3:87999000-87999200	Flanking Active TSS	Primary B cells from cord blood	blood

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