Variant report

Variant	rs4572791
Chromosome Location	chr3:89839503-89839504
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:89829884..89832447-chr3:89837199..89839743,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10511146	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11915486	0.82[EUR][1000 genomes]
rs11921883	0.85[ASN][1000 genomes]
rs12630314	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12631105	0.85[ASN][1000 genomes]
rs12636191	0.89[EUR][1000 genomes]
rs12638502	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1357169	0.89[EUR][1000 genomes]
rs17027183	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17027200	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17027205	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17027214	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17027245	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1915727	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1915728	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1915732	0.81[EUR][1000 genomes]
rs1949586	0.82[EUR][1000 genomes]
rs1949650	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2030397	0.82[EUR][1000 genomes]
rs4435660	0.82[EUR][1000 genomes]
rs55976185	0.82[EUR][1000 genomes]
rs57036056	0.85[ASN][1000 genomes]
rs6551423	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6771600	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6773084	0.89[EUR][1000 genomes]
rs6781309	0.85[ASN][1000 genomes]
rs6784293	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6786656	0.83[EUR][1000 genomes]
rs6787938	0.82[EUR][1000 genomes]
rs6806076	0.84[EUR][1000 genomes]
rs6806871	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72912050	0.85[ASN][1000 genomes]
rs72912076	0.82[EUR][1000 genomes]
rs72912079	0.82[EUR][1000 genomes]
rs72914067	0.81[EUR][1000 genomes]
rs7612414	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7641424	0.82[EUR][1000 genomes]
rs7652965	0.82[EUR][1000 genomes]
rs9683159	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008018	chr3:89382031-90254063	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv536639	chr3:89382031-90254063	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1010932	chr3:89424428-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1010021	chr3:89521983-90141988	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv530024	chr3:89548440-90304841	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv869889	chr3:89653238-90087372	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1013502	chr3:89670525-89915342	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv536641	chr3:89670525-89915342	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv834761	chr3:89718508-89877335	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1005444	chr3:89803641-90030755	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1008130	chr3:89837442-90192503	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:89839400-89840200	Enhancers	Stomach Mucosa	stomach

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