Variant report

Variant	rs10170094
Chromosome Location	chr2:141614663-141614664
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10179410	0.88[CEU][hapmap];0.88[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10204756	0.88[CEU][hapmap];0.80[CHB][hapmap];0.94[JPT][hapmap]
rs10204820	1.00[CEU][hapmap];0.89[JPT][hapmap]
rs1157026	0.88[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs12474883	1.00[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12691575	0.82[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs12691577	0.88[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap]
rs12691578	0.88[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap]
rs1429350	0.81[JPT][hapmap]
rs1429352	0.88[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1429359	0.89[JPT][hapmap];0.95[YRI][hapmap]
rs1864278	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.81[YRI][hapmap]
rs1978637	0.88[CEU][hapmap];0.81[CHB][hapmap];0.95[JPT][hapmap]
rs2029156	0.92[ASN][1000 genomes]
rs2033290	0.91[JPT][hapmap]
rs2220257	0.87[LWK][hapmap];0.80[MKK][hapmap];0.86[TSI][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes]
rs4954676	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];0.96[GIH][hapmap];0.80[JPT][hapmap];0.97[LWK][hapmap];0.94[MEX][hapmap];0.86[MKK][hapmap];0.96[TSI][hapmap];0.96[YRI][hapmap]
rs6429850	0.88[CEU][hapmap];0.88[CHB][hapmap];0.92[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7349387	0.88[CEU][hapmap];0.88[CHB][hapmap];0.92[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7565456	0.82[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs984013	0.88[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap]
rs996598	0.88[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1003008	chr2:141518795-141763505	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141614400-141617800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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