Variant report

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

rs_ID	r²[population]
rs1343600	0.81[ASN][1000 genomes]
rs1343606	0.81[ASN][1000 genomes]
rs1891948	0.85[AMR][1000 genomes]
rs2226195	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2799338	0.81[ASN][1000 genomes]
rs2799340	0.81[ASN][1000 genomes]
rs2799341	0.81[ASN][1000 genomes]
rs2799346	0.99[EUR][1000 genomes]
rs2799348	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2806938	0.81[ASN][1000 genomes]
rs2806948	0.81[ASN][1000 genomes]
rs2806961	0.81[ASN][1000 genomes]
rs2806962	0.81[ASN][1000 genomes]
rs2806967	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2806999	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2807002	0.86[AMR][1000 genomes]
rs2807004	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4884340	0.80[ASN][1000 genomes]
rs4886137	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7322978	0.81[ASN][1000 genomes]
rs7323451	0.81[ASN][1000 genomes]
rs9536346	0.86[CHB][hapmap];0.85[CHD][hapmap]
rs9568800	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530719	chr13:53173014-53675953	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv3440613	chr13:53307609-53671072	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv832613	chr13:53524319-53687188	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53633200-53642200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:53635600-53641600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr13:53636200-53641600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr13:53636200-53642400	Weak transcription	Brain Anterior Caudate	brain
5	chr13:53636400-53642200	Weak transcription	Brain Hippocampus Middle	brain
6	chr13:53636600-53642000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr13:53636600-53642200	Weak transcription	Brain Angular Gyrus	brain
8	chr13:53636800-53641600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:53637600-53641600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:53637800-53641000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr13:53639000-53642600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr13:53639200-53654800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr13:53639600-53642200	Weak transcription	Brain Germinal Matrix	brain
14	chr13:53639600-53643000	Weak transcription	Pancreas	Pancrea

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