Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10236653	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs10499442	0.89[CEU][hapmap]
rs11767890	0.85[CEU][hapmap]
rs12669548	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12674261	0.88[CEU][hapmap]
rs12699617	0.82[CEU][hapmap]
rs12699622	0.88[CEU][hapmap]
rs13221160	0.80[EUR][1000 genomes]
rs1431521	0.89[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1431528	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1560576	0.96[CEU][hapmap]
rs182034	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs1835675	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1897300	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs196751	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs196756	0.84[ASN][1000 genomes]
rs1991685	0.88[CEU][hapmap]
rs2052980	0.82[CEU][hapmap]
rs3823843	0.88[CEU][hapmap]
rs4370419	0.89[CEU][hapmap]
rs6461104	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6958691	0.81[CEU][hapmap]
rs7777633	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7794432	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7802759	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7807072	0.89[CEU][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs987448	0.92[CEU][hapmap]
rs987449	0.88[CEU][hapmap]

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	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
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14459600-14465000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:14459600-14465200	Weak transcription	Fetal Heart	heart
3	chr7:14462400-14462600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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