Variant report

Variant	rs2275727
Chromosome Location	chr10:26409836-26409837
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10508711	1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10508712	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10764599	0.82[ASN][1000 genomes]
rs10828939	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10828941	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10828944	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10828949	0.94[CEU][hapmap];0.81[CHB][hapmap];0.81[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10828950	1.00[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10828951	1.00[CEU][hapmap];0.85[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10828954	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10828957	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10828958	0.88[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10828961	0.85[ASN][1000 genomes]
rs10828962	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs11014917	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11014919	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11014930	0.92[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11014953	1.00[CEU][hapmap];0.95[CHB][hapmap];0.80[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11014954	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11014955	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11014960	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11014983	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11527599	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11599503	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12219979	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12269307	0.94[CEU][hapmap];0.90[CHB][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12571378	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12573019	0.94[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12764197	0.82[CEU][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12773851	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12774203	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12775931	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12779517	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12781541	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1339811	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1339819	0.82[CEU][hapmap]
rs1361713	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[JPT][hapmap];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17752077	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17752353	0.88[CEU][hapmap];0.90[CHB][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1935483	1.00[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1996715	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2000255	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2176938	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28796333	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2887177	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34240977	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34966498	0.85[EUR][1000 genomes]
rs3737316	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3817416	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3818957	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3824706	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4526683	0.94[CEU][hapmap];0.89[CHB][hapmap];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4747546	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4749090	0.82[CEU][hapmap]
rs4749092	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4749094	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4749098	0.88[CEU][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6482535	0.94[CEU][hapmap];0.90[CHB][hapmap];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7083144	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7083433	0.93[ASN][1000 genomes]
rs7905083	0.95[CHB][hapmap];0.84[ASN][1000 genomes]
rs7908081	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7915636	0.94[CEU][hapmap];0.90[CHB][hapmap];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9787562	0.82[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26402000-26436200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26409000-26410000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:26409800-26410200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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