Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11076316	0.85[AFR][1000 genomes]
rs11076320	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12444436	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12596240	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12599241	0.87[AFR][1000 genomes]
rs1582316	0.89[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs1582318	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1582321	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1582323	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1582325	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1582327	0.97[EUR][1000 genomes]
rs1592481	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1592488	0.90[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs1600002	0.90[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1600003	0.80[EUR][1000 genomes]
rs1861325	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1861326	0.98[EUR][1000 genomes]
rs1861327	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1861328	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2059233	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2216741	0.85[AFR][1000 genomes]
rs3743794	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs9635511	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492248	chr16:51681902-52456082	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv34024	chr16:51878565-52316530	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv827650	chr16:52067728-52124369	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1058257	chr16:52093549-52271815	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:52101400-52110400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr16:52101600-52107600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr16:52103000-52106600	Weak transcription	Fetal Lung	lung
4	chr16:52103000-52112600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr16:52104200-52108200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr16:52104200-52112600	Weak transcription	Brain Angular Gyrus	brain
7	chr16:52104200-52112600	Weak transcription	Brain Inferior Temporal Lobe	brain

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