Variant report

Variant	rs10469656
Chromosome Location	chr2:212486350-212486351
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10177211	0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs10177258	0.83[EUR][1000 genomes]
rs10497949	0.89[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10804200	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12104775	0.83[EUR][1000 genomes]
rs12469375	0.83[ASW][hapmap];1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs12616462	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12694246	0.91[ASN][1000 genomes]
rs1829611	0.82[MEX][hapmap]
rs1829612	0.83[ASN][1000 genomes]
rs1829613	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1851175	0.93[ASN][1000 genomes]
rs1851176	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1851177	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes]
rs1851190	0.89[CEU][hapmap];0.83[ASN][1000 genomes]
rs1851194	0.89[CEU][hapmap];0.87[CHB][hapmap];0.88[GIH][hapmap]
rs1851196	0.86[JPT][hapmap];0.83[EUR][1000 genomes]
rs1851197	0.83[EUR][1000 genomes]
rs1851198	0.83[EUR][1000 genomes]
rs1851199	0.83[EUR][1000 genomes]
rs3863853	0.86[ASN][1000 genomes]
rs4672620	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4673625	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7349376	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7559679	0.89[CEU][hapmap];0.93[JPT][hapmap];0.82[MEX][hapmap]
rs7565192	0.97[ASN][1000 genomes]
rs7580963	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7593315	0.84[ASN][1000 genomes]
rs7601664	0.83[ASW][hapmap];1.00[CEU][hapmap];0.94[GIH][hapmap];0.92[TSI][hapmap];0.92[EUR][1000 genomes]
rs9288436	0.80[CHB][hapmap];0.85[JPT][hapmap];0.81[EUR][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	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
2	esv2754366	chr2:212470494-212541494	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding 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	chr2:212467400-212546800	Weak transcription	Aorta	Aorta
2	chr2:212470400-212489600	Weak transcription	Fetal Heart	heart
3	chr2:212483000-212487800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:212484200-212488400	Weak transcription	HUVEC	blood vessel

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