Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10515220	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17084355	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs211514	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2194944	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2217060	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs295206	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs295208	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs309806	0.87[ASN][1000 genomes]
rs309808	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34112411	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs34838199	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs35270609	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs381984	0.84[ASN][1000 genomes]
rs384495	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs433273	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs450767	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4869226	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62364694	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62364697	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62364698	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62364699	0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7732965	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756469	chr5:94323268-94400017	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94319800-94346600	Weak transcription	HUVEC	blood vessel
2	chr5:94320400-94348000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:94334800-94353400	Weak transcription	Gastric	stomach
4	chr5:94334800-94358200	Weak transcription	Stomach Mucosa	stomach
5	chr5:94337400-94343200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:94337600-94341400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
7	chr5:94337800-94346800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr5:94338200-94339600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:94339000-94339800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:94339000-94343200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
11	chr5:94339000-94343400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
12	chr5:94339200-94339600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:94339200-94339600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
14	chr5:94339400-94341000	ZNF genes & repeats	Primary T cells from cord blood	blood
15	chr5:94339400-94341400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood

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