Variant report

Variant	rs10203022
Chromosome Location	chr2:212458790-212458791
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10177211	0.84[AMR][1000 genomes]
rs10177258	0.88[AMR][1000 genomes]
rs10204337	0.95[ASN][1000 genomes]
rs10210942	0.81[EUR][1000 genomes]
rs10804199	0.93[EUR][1000 genomes]
rs10932387	1.00[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10932388	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11684753	0.88[ASN][1000 genomes]
rs12465773	0.81[EUR][1000 genomes]
rs12619171	0.83[GIH][hapmap];0.94[MKK][hapmap]
rs12694244	0.88[ASN][1000 genomes]
rs1829610	0.81[YRI][hapmap];0.81[AFR][1000 genomes]
rs1829611	0.88[ASW][hapmap];1.00[GIH][hapmap];0.98[LWK][hapmap];0.82[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1851196	0.92[TSI][hapmap]
rs1972143	0.89[GIH][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs4539738	0.92[ASN][1000 genomes]
rs6746549	0.91[ASN][1000 genomes]
rs7556879	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.91[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7559679	0.83[TSI][hapmap]
rs7559734	0.91[ASN][1000 genomes]
rs7585825	0.88[ASN][1000 genomes]
rs7586137	0.83[ASW][hapmap];0.81[CHB][hapmap];0.83[GIH][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs7589006	0.81[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7602185	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7602757	0.89[ASN][1000 genomes]
rs7602850	0.89[ASN][1000 genomes]
rs9288434	0.81[EUR][1000 genomes]
rs9288435	0.89[GIH][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs9288436	0.83[ASW][hapmap];0.86[LWK][hapmap];0.85[MKK][hapmap];0.92[TSI][hapmap];0.80[AFR][1000 genomes]
rs939591	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000722	chr2:212272622-212465143	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv460069	chr2:212415948-212471642	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv584320	chr2:212415948-212471642	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv584321	chr2:212446818-212511895	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212452400-212466800	Weak transcription	Aorta	Aorta
2	chr2:212456600-212473600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:212458000-212458800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:212458000-212458800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:212458200-212463000	Weak transcription	Fetal Heart	heart

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