Variant report

Variant	rs4928134
Chromosome Location	chr3:99191076-99191077
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10511174	0.88[EUR][1000 genomes]
rs13063175	0.88[EUR][1000 genomes]
rs13064696	0.94[EUR][1000 genomes]
rs13070584	0.83[EUR][1000 genomes]
rs13084282	0.88[EUR][1000 genomes]
rs13086098	0.88[EUR][1000 genomes]
rs13088964	0.88[EUR][1000 genomes]
rs13098261	0.83[EUR][1000 genomes]
rs16841321	0.88[EUR][1000 genomes]
rs16841339	0.88[EUR][1000 genomes]
rs34060873	0.95[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs34162135	0.88[EUR][1000 genomes]
rs34201317	0.97[EUR][1000 genomes]
rs34468147	0.88[EUR][1000 genomes]
rs34580839	0.88[EUR][1000 genomes]
rs34686662	0.97[EUR][1000 genomes]
rs34964323	0.88[EUR][1000 genomes]
rs35217023	0.88[EUR][1000 genomes]
rs35479623	0.97[EUR][1000 genomes]
rs35722344	0.88[EUR][1000 genomes]
rs35787037	0.95[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs35892771	0.88[EUR][1000 genomes]
rs35981855	0.97[EUR][1000 genomes]
rs36015505	0.88[EUR][1000 genomes]
rs4928201	0.86[EUR][1000 genomes]
rs6765840	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs71313551	0.88[EUR][1000 genomes]
rs71313553	0.81[EUR][1000 genomes]
rs71313554	0.88[EUR][1000 genomes]
rs71313556	0.88[EUR][1000 genomes]
rs7629812	0.88[EUR][1000 genomes]
rs7630545	0.88[EUR][1000 genomes]
rs7649391	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv530026	chr3:98837320-99340537	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv3916	chr3:99186008-99232052	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:99187800-99191200	Weak transcription	HSMMtube	muscle
2	chr3:99188600-99192400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:99188800-99192000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:99189200-99194600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:99189600-99192000	Enhancers	Osteobl	bone
6	chr3:99189800-99191800	Enhancers	NHDF-Ad	bronchial
7	chr3:99190600-99191800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:99190600-99193200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:99190800-99192200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr3:99190800-99192200	Enhancers	NHLF	lung
11	chr3:99190800-99192400	Enhancers	Adipose Nuclei	Adipose
12	chr3:99190800-99194000	Enhancers	HSMM	muscle
13	chr3:99191000-99192000	Weak transcription	Aorta	Aorta

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