Variant report

Variant	rs1515289
Chromosome Location	chr2:180551664-180551665
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	chr2:180545707..180548071-chr2:180550130..180552377,2	K562	blood:
2	chr2:180545732..180548071-chr2:180550130..180552936,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10208354	0.94[ASN][1000 genomes]
rs1022311	0.94[CHB][hapmap];0.85[JPT][hapmap]
rs10497544	0.94[CHB][hapmap];0.91[JPT][hapmap]
rs10930882	0.89[CEU][hapmap]
rs11686166	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11690551	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs11901346	0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12373725	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12622727	0.94[CHB][hapmap];0.86[JPT][hapmap]
rs12623583	0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs13406795	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13419649	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13427033	1.00[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs1515281	0.83[JPT][hapmap]
rs1515282	0.85[JPT][hapmap]
rs1515287	0.86[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1515288	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs16866903	0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs16866915	0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs17820975	0.88[ASN][1000 genomes]
rs2292652	0.93[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs3106689	0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs3106725	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs3112968	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs3112970	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs34714722	0.89[ASN][1000 genomes]
rs58011887	0.81[ASN][1000 genomes]
rs62175163	0.84[ASN][1000 genomes]
rs62175164	0.85[ASN][1000 genomes]
rs62175165	0.85[ASN][1000 genomes]
rs62177571	0.80[ASN][1000 genomes]
rs7421557	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs7558364	1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs7558784	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7585817	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7585897	0.85[ASN][1000 genomes]
rs7590028	0.81[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs932113	0.94[CHB][hapmap];0.93[JPT][hapmap]
rs932115	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.91[AFR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs956261	0.94[CHB][hapmap];0.93[JPT][hapmap]
rs9989898	0.96[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180540400-180571200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180544000-180557200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:180551000-180552600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:180551200-180553000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:180551600-180552200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:180551600-180552400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:180551600-180552400	Enhancers	Muscle Satellite Cultured Cells	--

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