Variant report

Variant	rs9808364
Chromosome Location	chr2:134078664-134078665
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	chr2:134072524..134074621-chr2:134077160..134080145,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10182402	0.99[ASN][1000 genomes]
rs10191826	0.81[ASN][1000 genomes]
rs10469580	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10928450	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10928451	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11884182	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13392963	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13406057	0.81[ASN][1000 genomes]
rs13407503	0.81[ASN][1000 genomes]
rs13414823	0.99[ASN][1000 genomes]
rs13432602	0.86[ASN][1000 genomes]
rs1430165	0.97[ASN][1000 genomes]
rs1430166	0.81[ASN][1000 genomes]
rs2115864	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2289075	0.82[ASN][1000 genomes]
rs28415460	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4588241	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57942569	0.97[ASN][1000 genomes]
rs58035542	0.97[ASN][1000 genomes]
rs59037048	0.96[ASN][1000 genomes]
rs62180011	0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs62180012	0.82[ASN][1000 genomes]
rs6724854	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6724865	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9808392	0.99[ASN][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	nsv997821	chr2:133868822-134360220	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535927	chr2:133868822-134360220	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1002488	chr2:133890159-134275312	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv535928	chr2:133890159-134275312	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	esv3375790	chr2:133906915-134222833	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv834384	chr2:134005229-134188648	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv1003964	chr2:134039363-134088319	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1014718	chr2:134067133-134151633	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr2:134070200-134082200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:134070400-134094600	Weak transcription	NHEK	skin
3	chr2:134071200-134081600	Weak transcription	Right Ventricle	heart
4	chr2:134075800-134081000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:134076200-134081000	Weak transcription	Hela-S3	cervix
6	chr2:134078200-134079200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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