Variant report

Variant	rs10059820
Chromosome Location	chr5:124366575-124366576
allele	A/G
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:33)

rs_ID	r²[population]
rs10036117	0.83[EUR][1000 genomes]
rs10037351	0.83[EUR][1000 genomes]
rs10039152	0.83[EUR][1000 genomes]
rs10051515	0.83[EUR][1000 genomes]
rs10051816	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10051865	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10056903	0.83[EUR][1000 genomes]
rs10059682	0.83[EUR][1000 genomes]
rs10061638	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10065416	0.83[EUR][1000 genomes]
rs10076719	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10076822	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10223088	0.83[EUR][1000 genomes]
rs10478646	0.83[EUR][1000 genomes]
rs28379635	1.00[EUR][1000 genomes]
rs28421593	0.83[EUR][1000 genomes]
rs28442881	0.83[EUR][1000 genomes]
rs28469490	0.83[EUR][1000 genomes]
rs56878962	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60081045	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60582094	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6862844	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6862998	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6867051	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6867249	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6870217	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6874077	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6874416	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6875818	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6891699	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73306728	0.83[EUR][1000 genomes]
rs73306768	0.83[EUR][1000 genomes]
rs73308739	1.00[EUR][1000 genomes]

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	nsv882822	chr5:124250018-124449375	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830474	chr5:124263628-124431299	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124363000-124368000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr5:124363000-124368200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:124363400-124367000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:124363400-124367800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr5:124363400-124367800	Weak transcription	Gastric	stomach
6	chr5:124363400-124377600	Weak transcription	Fetal Kidney	kidney
7	chr5:124363600-124367600	Weak transcription	Adipose Nuclei	Adipose
8	chr5:124363600-124370000	Weak transcription	Stomach Mucosa	stomach
9	chr5:124365400-124379400	Weak transcription	Pancreas	Pancrea
10	chr5:124365800-124369600	Weak transcription	Duodenum Mucosa	Duodenum

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