Variant report

Variant	rs9567865
Chromosome Location	chr13:48010951-48010952
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10507558	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11617662	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11618099	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11618168	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12585227	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1340342	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1340343	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1340344	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2406331	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4131976	0.80[EUR][1000 genomes]
rs4257112	0.81[EUR][1000 genomes]
rs4284535	0.82[EUR][1000 genomes]
rs4303377	0.81[EUR][1000 genomes]
rs4368074	0.91[EUR][1000 genomes]
rs4383047	0.81[EUR][1000 genomes]
rs4470048	0.82[EUR][1000 genomes]
rs4622408	0.81[EUR][1000 genomes]
rs4941592	0.82[EUR][1000 genomes]
rs4942642	0.82[EUR][1000 genomes]
rs59309287	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61083113	0.93[ASN][1000 genomes]
rs7317842	0.92[ASN][1000 genomes]
rs7337528	0.89[ASN][1000 genomes]
rs7984261	0.82[EUR][1000 genomes]
rs7984310	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7988780	0.83[ASN][1000 genomes]
rs7994481	0.88[ASN][1000 genomes]
rs9316293	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9316294	0.93[ASN][1000 genomes]
rs9526339	0.81[EUR][1000 genomes]
rs9526340	0.84[CEU][hapmap];0.83[CHB][hapmap];0.81[JPT][hapmap];0.80[EUR][1000 genomes]
rs9526342	0.80[EUR][1000 genomes]
rs9534638	0.90[ASN][1000 genomes]
rs9534658	0.81[EUR][1000 genomes]
rs9534659	0.81[EUR][1000 genomes]
rs9534662	0.80[EUR][1000 genomes]
rs9534663	0.80[EUR][1000 genomes]
rs9534664	0.80[EUR][1000 genomes]
rs9567854	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9567856	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9567872	0.81[EUR][1000 genomes]
rs9591064	0.84[ASN][1000 genomes]

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	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3450125	chr13:47919050-48236684	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv455879	chr13:47919611-48190106	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv561588	chr13:47943829-48190106	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr13:48007400-48011400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr13:48007800-48012000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:48008000-48011000	Weak transcription	NHDF-Ad	bronchial

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