Variant report

Variant	rs4660960
Chromosome Location	chr1:47287766-47287767
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:47282268..47284457-chr1:47286910..47288924,2	K562	blood:

Variant related genes	Relation type
ENSG00000142973	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11211366	0.86[ASN][1000 genomes]
rs11211369	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11211386	0.88[EUR][1000 genomes]
rs11211387	0.89[EUR][1000 genomes]
rs1122582	0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11576162	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11583378	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11584320	0.89[EUR][1000 genomes]
rs11586184	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12402717	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12410657	0.96[EUR][1000 genomes]
rs12566735	0.89[EUR][1000 genomes]
rs12569216	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1572603	0.90[EUR][1000 genomes]
rs1890246	0.90[EUR][1000 genomes]
rs1890248	0.90[EUR][1000 genomes]
rs1890249	0.90[EUR][1000 genomes]
rs2185032	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2405335	0.84[ASN][1000 genomes]
rs3766195	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3766196	0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3766197	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3820080	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3863632	0.84[EUR][1000 genomes]
rs4417002	0.89[EUR][1000 genomes]
rs45563134	0.86[ASN][1000 genomes]
rs4560983	0.80[EUR][1000 genomes]
rs4646482	0.84[ASN][1000 genomes]
rs4646486	0.96[EUR][1000 genomes]
rs4646487	0.83[EUR][1000 genomes]
rs4646492	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4646493	0.85[EUR][1000 genomes]
rs4646495	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55868139	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55936777	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60430993	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61741519	0.84[EUR][1000 genomes]
rs67678353	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72637963	0.96[EUR][1000 genomes]
rs72681939	0.92[EUR][1000 genomes]
rs751027	0.83[ASN][1000 genomes]
rs7553652	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs837395	0.83[ASN][1000 genomes]
rs9728536	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1013048	chr1:47132831-47377364	Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv534955	chr1:47132831-47377364	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1011086	chr1:47259078-47305191	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv870538	chr1:47259138-47309265	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1004143	chr1:47270942-47321982	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1004246	chr1:47274901-47321982	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv947111	chr1:47277189-47308420	ZNF genes & repeats Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	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	chr1:47286000-47288400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:47286600-47287800	Weak transcription	Right Ventricle	heart
3	chr1:47286600-47288000	Weak transcription	Adipose Nuclei	Adipose
4	chr1:47286600-47288200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr1:47286600-47288200	Weak transcription	Right Atrium	heart
6	chr1:47286600-47296400	Weak transcription	Lung	lung
7	chr1:47286800-47288000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:47286800-47288200	Weak transcription	Left Ventricle	heart
9	chr1:47286800-47296200	Weak transcription	Esophagus	oesophagus

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