Variant report

Variant	rs6855053
Chromosome Location	chr4:55032723-55032724
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11932776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35249513	1.00[AMR][1000 genomes]
rs57735051	1.00[AMR][1000 genomes]
rs58366718	1.00[AMR][1000 genomes]
rs60313972	1.00[AMR][1000 genomes]
rs60398195	1.00[AMR][1000 genomes]
rs6838383	1.00[AMR][1000 genomes]
rs6848460	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73149594	1.00[AMR][1000 genomes]
rs73151406	1.00[AMR][1000 genomes]
rs73151429	1.00[AMR][1000 genomes]
rs73151433	1.00[AMR][1000 genomes]
rs73151456	1.00[AMR][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	nsv1003167	chr4:54732051-55081905	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv537096	chr4:54732051-55081905	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats 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	nsv879020	chr4:54986912-55064573	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv523058	chr4:55018617-55045716	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55018800-55036200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:55030600-55033000	Enhancers	HSMM	muscle
3	chr4:55031600-55036200	Weak transcription	Aorta	Aorta
4	chr4:55032000-55033000	Enhancers	NH-A	brain
5	chr4:55032000-55037000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:55032200-55033000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:55032400-55035200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr4:55032400-55035200	Weak transcription	HSMMtube	muscle
9	chr4:55032400-55035400	Weak transcription	Osteobl	bone
10	chr4:55032400-55039600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr4:55032600-55033800	Weak transcription	NHEK	skin
12	chr4:55032600-55035200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:55032600-55035200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:55032600-55035400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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Input of quick search could be:

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

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