Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10003344	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11728684	0.88[ASN][1000 genomes]
rs13131341	0.84[EUR][1000 genomes]
rs1365624	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1820521	0.83[EUR][1000 genomes]
rs1820522	0.83[EUR][1000 genomes]
rs1834693	0.84[EUR][1000 genomes]
rs2256669	0.82[EUR][1000 genomes]
rs2332893	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2555648	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2555665	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2612653	0.88[ASN][1000 genomes]
rs2612664	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2612671	0.86[EUR][1000 genomes]
rs2612676	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4147099	0.84[EUR][1000 genomes]
rs4365703	0.85[EUR][1000 genomes]
rs4695933	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73012605	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7656557	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9997598	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][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	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv881376	chr4:175466101-175513812	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175466600-175484600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:175471600-175476600	Weak transcription	Stomach Mucosa	stomach
3	chr4:175472200-175475400	Weak transcription	Fetal Stomach	stomach
4	chr4:175473400-175476800	Weak transcription	Fetal Intestine Small	intestine
5	chr4:175473400-175478400	Weak transcription	Placenta	Placenta
6	chr4:175474000-175476000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:175474200-175475800	Enhancers	NHDF-Ad	bronchial
8	chr4:175474200-175475800	Enhancers	NHEK	skin
9	chr4:175474200-175476000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:175474600-175475000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:175474600-175476000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:175474800-175475000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:175474800-175476000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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