Variant report

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

rs_ID	r²[population]
rs10228492	0.91[AFR][1000 genomes]
rs10257651	0.81[AFR][1000 genomes]
rs17168038	1.00[CEU][hapmap]
rs17168042	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2108514	0.90[YRI][hapmap];0.84[AFR][1000 genomes]
rs2108515	0.86[YRI][hapmap];0.89[AFR][1000 genomes]
rs2190672	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4483055	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55776849	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55816754	0.89[AFR][1000 genomes]
rs56752869	0.86[ASN][1000 genomes]
rs57360595	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60170162	1.00[EUR][1000 genomes]
rs62443703	0.94[ASN][1000 genomes]
rs62443937	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6944473	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6962605	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6970467	0.82[AFR][1000 genomes]
rs6975629	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs7793052	0.86[YRI][hapmap];0.90[AFR][1000 genomes]
rs7796825	0.87[YRI][hapmap];0.90[AFR][1000 genomes]
rs7797910	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr7:14325600-14327200	Weak transcription	Fetal Heart	heart

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