Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10864183	0.85[CHB][hapmap];0.89[JPT][hapmap]
rs11120598	0.80[CHB][hapmap];0.88[JPT][hapmap]
rs11578710	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs12122359	0.94[EUR][1000 genomes]
rs12403674	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs12404185	0.94[EUR][1000 genomes]
rs2364859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2820675	0.86[CHB][hapmap];0.89[JPT][hapmap]
rs2820692	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs2820693	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs2820694	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs2820696	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs2886198	0.87[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs2886199	0.83[CEU][hapmap];0.83[JPT][hapmap]
rs3845525	0.93[EUR][1000 genomes]
rs3845527	0.83[CEU][hapmap];0.89[JPT][hapmap];0.93[EUR][1000 genomes]
rs4372227	0.84[CEU][hapmap]
rs4375233	0.84[CEU][hapmap];0.89[JPT][hapmap]
rs4375237	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs4628479	0.84[CEU][hapmap];0.89[JPT][hapmap];0.94[YRI][hapmap]
rs4655423	0.89[JPT][hapmap]
rs57472918	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61828172	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6665313	0.83[CEU][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap]
rs7546433	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[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	nsv430324	chr1:215649163-216082605	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv873171	chr1:215825167-215925167	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 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	chr1:215878200-215883600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:215882000-215882200	Enhancers	Gastric	stomach
3	chr1:215882000-215882200	Enhancers	Pancreas	Pancrea
4	chr1:215882000-215884200	Enhancers	Liver	Liver

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