Variant report

Variant	rs6778188
Chromosome Location	chr3:155037601-155037602
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:15)

rs_ID	r²[population]
rs1056670	0.94[ASN][1000 genomes]
rs1134899	0.94[ASN][1000 genomes]
rs62279092	0.94[ASN][1000 genomes]
rs62279095	0.94[ASN][1000 genomes]
rs62279096	0.94[ASN][1000 genomes]
rs62279098	0.94[ASN][1000 genomes]
rs62279099	0.94[ASN][1000 genomes]
rs62279100	0.94[ASN][1000 genomes]
rs62279128	0.94[ASN][1000 genomes]
rs62279129	0.94[ASN][1000 genomes]
rs62279130	0.94[ASN][1000 genomes]
rs6792632	0.94[ASN][1000 genomes]
rs6792930	0.94[ASN][1000 genomes]
rs7637871	0.94[ASN][1000 genomes]
rs7649809	0.91[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	nsv999994	chr3:154579254-155175303	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv532664	chr3:154588346-155162615	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv1000753	chr3:154848433-155207022	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv536773	chr3:154848433-155207022	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv829762	chr3:154879350-155052986	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr3:155032000-155040000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:155033400-155040000	Weak transcription	Psoas Muscle	Psoas
3	chr3:155034600-155039200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr3:155035600-155039000	Weak transcription	NHDF-Ad	bronchial
5	chr3:155036400-155039400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:155036600-155039000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:155037200-155043800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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