Variant report

Variant	rs368255
Chromosome Location	chr3:21474689-21474690
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12638887	0.81[CHB][hapmap]
rs2076829	0.83[CHB][hapmap]
rs341850	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs341852	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs341853	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs341854	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3732905	0.80[CEU][hapmap];0.89[CHB][hapmap]
rs3821733	0.93[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3849537	0.92[CEU][hapmap];0.88[CHB][hapmap];0.89[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3849539	0.80[CEU][hapmap];0.89[CHB][hapmap]
rs3860572	0.89[CHB][hapmap]
rs400737	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs453364	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4857999	0.80[CEU][hapmap];0.94[CHB][hapmap]
rs4858000	0.80[CEU][hapmap];0.94[CHB][hapmap]
rs4858002	0.80[CEU][hapmap];0.94[CHB][hapmap]
rs6550607	0.94[CHB][hapmap]
rs6774929	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6787456	0.80[CEU][hapmap];0.94[CHB][hapmap]
rs6787955	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6797692	0.94[CHB][hapmap]
rs6806788	0.88[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs7611710	0.89[CHB][hapmap]
rs7614523	0.88[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs7625365	0.89[CHB][hapmap]
rs7643842	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs9809197	0.89[CHB][hapmap]
rs9838377	0.84[ASN][1000 genomes]
rs9874351	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9879872	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834630	chr3:21311619-21491327	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1006471	chr3:21385627-21596955	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1000828	chr3:21399870-21565580	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv536515	chr3:21399870-21565580	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21453200-21475600	Weak transcription	Fetal Muscle Leg	muscle
2	chr3:21458800-21483400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr3:21459200-21477200	Weak transcription	Fetal Lung	lung
4	chr3:21460200-21474800	Weak transcription	NHDF-Ad	bronchial
5	chr3:21463000-21491400	Weak transcription	Aorta	Aorta
6	chr3:21469200-21475800	Weak transcription	Fetal Stomach	stomach
7	chr3:21474600-21475200	Enhancers	Brain Germinal Matrix	brain
8	chr3:21474600-21478400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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