Variant report

Variant	rs10226465
Chromosome Location	chr7:50916316-50916317
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:50906192..50908348-chr7:50915043..50917108,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10230084	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10233389	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs10234720	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10242300	0.86[EUR][1000 genomes]
rs10250894	0.86[EUR][1000 genomes]
rs10267953	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10282345	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12718959	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12718961	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17454517	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17564264	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1862946	0.86[EUR][1000 genomes]
rs1862948	0.86[EUR][1000 genomes]
rs4947934	0.83[ASN][1000 genomes]
rs4947936	0.86[EUR][1000 genomes]
rs4947937	0.87[EUR][1000 genomes]
rs4947938	0.87[EUR][1000 genomes]
rs4947939	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4947945	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs6976298	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7350021	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7357209	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781924	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7802799	0.86[EUR][1000 genomes]
rs9656704	0.87[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	nsv1016665	chr7:50452552-51404524	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv606907	chr7:50899168-51195380	Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50907200-50916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:50911400-50925600	Weak transcription	Pancreas	Pancrea

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