Variant report

Variant	rs73117867
Chromosome Location	chr4:28374945-28374946
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1158230	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158231	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11935635	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11945645	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11947184	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16880558	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34890254	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58224835	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73115466	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73115468	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117858	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117862	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117864	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117866	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117869	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117870	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117875	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117878	0.96[EUR][1000 genomes]
rs73117880	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117883	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117887	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117890	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117891	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73804356	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7677693	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005382	chr4:28157180-28403800	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv878775	chr4:28163856-28473048	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1000514	chr4:28192982-28445194	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1012210	chr4:28246489-28419673	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1010133	chr4:28273244-28642942	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1014938	chr4:28277683-28642942	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1013013	chr4:28323465-28419673	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:28371600-28375000	Weak transcription	HMEC	breast
2	chr4:28371800-28375000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:28371800-28375000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:28371800-28375200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:28372200-28379400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:28374600-28376200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:28374800-28376600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:28374800-28377800	Enhancers	NHEK	skin

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