Variant report

Variant	rs17009533
Chromosome Location	chr10:49477904-49477905
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49475447..49477972-chr10:49481298..49483019,2	K562	blood:
2	chr10:49475447..49477971-chr10:49480331..49482798,2	K562	blood:

Variant related genes	Relation type
ENSG00000170324	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10508900	0.84[EUR][1000 genomes]
rs11816450	1.00[JPT][hapmap]
rs11819269	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs12246849	1.00[JPT][hapmap]
rs12262288	1.00[JPT][hapmap]
rs1465605	1.00[JPT][hapmap]
rs1652245	1.00[JPT][hapmap]
rs166815	1.00[JPT][hapmap]
rs166817	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs169439	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs17009537	1.00[CEU][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17009540	0.84[EUR][1000 genomes]
rs17009545	0.84[EUR][1000 genomes]
rs1730444	1.00[JPT][hapmap]
rs1730446	1.00[JPT][hapmap]
rs1881733	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1881734	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs204006	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2455321	1.00[JPT][hapmap]
rs2652408	1.00[JPT][hapmap]
rs2698764	1.00[JPT][hapmap]
rs280605	1.00[JPT][hapmap]
rs280606	1.00[JPT][hapmap]
rs280608	1.00[JPT][hapmap]
rs280610	1.00[JPT][hapmap]
rs280611	1.00[JPT][hapmap]
rs280612	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs386570	1.00[JPT][hapmap]
rs399419	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes]
rs413065	1.00[JPT][hapmap]
rs440943	1.00[JPT][hapmap]
rs477693	1.00[JPT][hapmap]
rs4838592	1.00[JPT][hapmap]
rs61840508	0.97[EUR][1000 genomes]
rs61840510	0.84[EUR][1000 genomes]
rs7073154	1.00[JPT][hapmap]
rs7092864	0.88[CEU][hapmap];1.00[JPT][hapmap]
rs73296380	0.97[EUR][1000 genomes]
rs7915333	0.86[CEU][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895366	chr10:49299274-49576454	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv895367	chr10:49333754-49491047	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv895368	chr10:49381635-49551560	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv467190	chr10:49402084-49576878	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv550811	chr10:49402084-49576878	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv895370	chr10:49421173-49484698	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr10:49466800-49492400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:49475000-49482600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:49475000-49482600	Weak transcription	Right Atrium	heart
4	chr10:49475000-49482800	Weak transcription	Pancreas	Pancrea
5	chr10:49477400-49479600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr10:49477800-49478000	Enhancers	Fetal Thymus	thymus

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