Variant report

Variant	rs10495988
Chromosome Location	chr2:50155935-50155936
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:50155376..50157219-chr2:50161102..50163078,2	MCF-7	breast:
2	chr2:50152142..50154281-chr2:50155561..50158371,2	K562	blood:
3	chr2:50154076..50156856-chr2:50160759..50162386,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1013597	0.89[CEU][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11125278	0.89[CEU][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11885824	0.89[CEU][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11902804	0.89[CEU][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12476729	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12617277	0.89[CEU][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.85[TSI][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12618646	0.89[CEU][hapmap];0.82[JPT][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12995774	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12998798	1.00[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13000689	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13007882	0.89[CEU][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13016321	0.89[CEU][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13022108	0.89[CEU][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13023203	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13023905	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13025974	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13028383	0.88[EUR][1000 genomes]
rs1345562	0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17039412	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17039430	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17039448	0.89[CEU][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.80[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17039452	1.00[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17039454	1.00[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17039456	0.89[CEU][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17039472	0.84[CEU][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17039484	0.89[CEU][hapmap];0.85[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17039508	0.81[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17039581	0.84[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.87[MKK][hapmap];0.83[TSI][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes]
rs17039592	0.85[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs2241750	0.89[CEU][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2241752	0.89[CEU][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34533417	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34918442	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35371642	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35373906	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3922898	0.87[EUR][1000 genomes]
rs3935314	0.88[EUR][1000 genomes]
rs4143112	0.84[CEU][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs57936567	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs60884569	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62132409	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62132414	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62132439	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62132441	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62132445	0.93[AMR][1000 genomes]
rs6745765	0.89[CEU][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.80[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6753652	0.82[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6758043	0.88[CEU][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6758276	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7598993	0.89[CEU][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs920033	0.88[CEU][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs920034	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs920035	0.86[CEU][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3388948	chr2:50092667-50602681	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3399511	chr2:50092687-50602651	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv934303	chr2:50145598-50412189	Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50141600-50175400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr2:50141600-50187400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:50149400-50156200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:50151800-50160600	Weak transcription	Fetal Heart	heart

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