Variant report

Variant	rs1909964
Chromosome Location	chr3:21496104-21496105
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:21491005..21492571-chr3:21495896..21498520,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs12497792	0.81[ASN][1000 genomes]
rs17008828	0.81[ASN][1000 genomes]
rs17273460	0.81[ASN][1000 genomes]
rs17273467	0.81[ASN][1000 genomes]
rs17273474	0.83[ASN][1000 genomes]
rs17273481	0.83[ASN][1000 genomes]
rs17273488	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1909963	0.90[ASN][1000 genomes]
rs365392	0.81[ASN][1000 genomes]
rs382006	0.80[ASN][1000 genomes]
rs390039	0.81[ASN][1000 genomes]
rs3911495	0.97[AFR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3911496	0.97[AFR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3913939	0.83[ASN][1000 genomes]
rs3913940	0.83[ASN][1000 genomes]
rs3913941	0.83[ASN][1000 genomes]
rs4045436	0.83[ASN][1000 genomes]
rs417269	0.81[ASN][1000 genomes]
rs424695	0.82[ASN][1000 genomes]
rs4263311	0.81[ASN][1000 genomes]
rs444724	0.89[ASN][1000 genomes]
rs446720	0.81[ASN][1000 genomes]
rs447169	0.81[ASN][1000 genomes]
rs453597	0.89[ASN][1000 genomes]
rs453990	0.81[ASN][1000 genomes]
rs4858324	0.83[ASN][1000 genomes]
rs4858325	0.81[ASN][1000 genomes]
rs4858326	0.83[ASN][1000 genomes]
rs55878001	0.83[ASN][1000 genomes]
rs55941003	0.82[ASN][1000 genomes]
rs56316641	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73042502	0.81[ASN][1000 genomes]
rs73044405	0.82[ASN][1000 genomes]
rs73044408	0.81[ASN][1000 genomes]
rs73044415	0.83[ASN][1000 genomes]
rs73044417	0.83[ASN][1000 genomes]
rs73044418	0.83[ASN][1000 genomes]
rs73044420	0.83[ASN][1000 genomes]
rs73044422	0.83[ASN][1000 genomes]
rs73044428	0.83[ASN][1000 genomes]
rs73044429	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006471	chr3:21385627-21596955	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1000828	chr3:21399870-21565580	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv536515	chr3:21399870-21565580	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1011226	chr3:21489712-21525789	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21477000-21507200	Weak transcription	Fetal Muscle Leg	muscle
2	chr3:21489200-21506600	Weak transcription	Fetal Stomach	stomach
3	chr3:21491600-21503200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:21491800-21506800	Weak transcription	Aorta	Aorta

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