Variant report

Variant	rs4682020
Chromosome Location	chr3:110490165-110490166
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10934065	0.86[EUR][1000 genomes]
rs1156743	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1156744	0.85[EUR][1000 genomes]
rs11715183	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1303902	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13077386	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs13098266	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1381604	0.86[EUR][1000 genomes]
rs1462301	0.86[EUR][1000 genomes]
rs1462314	0.86[EUR][1000 genomes]
rs1462315	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1585559	0.83[EUR][1000 genomes]
rs1599570	0.85[EUR][1000 genomes]
rs1599572	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1599574	0.84[EUR][1000 genomes]
rs17202466	0.86[EUR][1000 genomes]
rs2054375	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2126450	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2169496	0.84[EUR][1000 genomes]
rs2199454	0.89[CEU][hapmap]
rs2399357	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2399362	0.87[EUR][1000 genomes]
rs4234398	0.83[EUR][1000 genomes]
rs4610259	0.86[EUR][1000 genomes]
rs4640600	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4682019	0.83[EUR][1000 genomes]
rs4682204	0.83[EUR][1000 genomes]
rs4682205	0.87[EUR][1000 genomes]
rs4682206	0.87[EUR][1000 genomes]
rs4682207	0.91[EUR][1000 genomes]
rs56203101	0.86[EUR][1000 genomes]
rs6773268	0.83[EUR][1000 genomes]
rs6805801	0.88[EUR][1000 genomes]
rs7629191	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs7633234	0.87[EUR][1000 genomes]
rs7633936	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs7637286	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7647181	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7647421	0.86[EUR][1000 genomes]
rs9288913	0.87[EUR][1000 genomes]
rs931019	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9830854	0.86[EUR][1000 genomes]
rs9836371	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9837589	0.86[EUR][1000 genomes]
rs9857065	0.84[EUR][1000 genomes]
rs9857228	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9859534	0.87[EUR][1000 genomes]
rs991930	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001810	chr3:110158316-110522247	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1010230	chr3:110204439-110588814	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv536688	chr3:110204439-110588814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1011034	chr3:110209344-110559021	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536689	chr3:110209344-110559021	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv1014199	chr3:110293896-110754155	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv829673	chr3:110378069-110530815	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110471400-110492200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:110472600-110492400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:110486400-110492200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:110488000-110490800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:110489400-110490600	Weak transcription	Fetal Heart	heart
6	chr3:110490000-110494400	Enhancers	HepG2	liver

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