Variant report

Variant	rs820548
Chromosome Location	chr3:112473928-112473929
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11917839	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12489081	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12496168	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35106456	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3912626	0.91[EUR][1000 genomes]
rs59902023	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6781277	0.83[EUR][1000 genomes]
rs6781391	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6781496	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6781609	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6781823	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6806013	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72946393	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7614300	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7646744	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7646996	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432477	chr3:112390310-112603310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv877343	chr3:112470586-112597706	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112468000-112478200	Weak transcription	K562	blood
2	chr3:112468000-112488200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:112471200-112479400	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr3:112471200-112479600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:112472000-112474400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr3:112473400-112475200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr3:112473600-112475200	Enhancers	Primary monocytes fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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