Variant report

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

rs_ID	r²[population]
rs10517291	0.81[EUR][1000 genomes]
rs11947928	0.82[ASN][1000 genomes]
rs12499731	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12500564	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12512748	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17082549	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs17082565	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17082579	0.86[AMR][1000 genomes]
rs17082581	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35784764	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4864451	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4864452	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4864453	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4864454	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4864747	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6826467	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73147396	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73149212	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs751265	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7664488	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7687029	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9762074	0.86[AMR][1000 genomes];0.82[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	nsv997614	chr4:54086727-54150632	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv879013	chr4:54093717-54137228	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1008593	chr4:54120297-54207769	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 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	chr4:54101600-54129400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:54108400-54129600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:54114400-54134400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:54114400-54139600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:54114400-54144000	Weak transcription	Liver	Liver
6	chr4:54114600-54126400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr4:54114600-54129800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:54114800-54129400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:54114800-54130000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr4:54117800-54132800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:54119600-54130400	Weak transcription	NHLF	lung
12	chr4:54120600-54123200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:54120600-54124000	Weak transcription	Primary T cells from cord blood	blood
14	chr4:54122200-54139800	Weak transcription	Muscle Satellite Cultured Cells	--

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