Variant report

Variant	rs4241981
Chromosome Location	chr4:55038153-55038154
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17083988	1.00[EUR][1000 genomes]
rs17838983	1.00[EUR][1000 genomes]
rs4352534	1.00[EUR][1000 genomes]
rs58015793	1.00[EUR][1000 genomes]
rs58080484	1.00[EUR][1000 genomes]
rs60639295	1.00[EUR][1000 genomes]
rs61277389	1.00[EUR][1000 genomes]
rs61510049	1.00[EUR][1000 genomes]
rs6818057	1.00[EUR][1000 genomes]
rs73147749	1.00[EUR][1000 genomes]
rs73147754	1.00[EUR][1000 genomes]
rs73147760	1.00[EUR][1000 genomes]
rs73147772	1.00[EUR][1000 genomes]
rs73147780	1.00[EUR][1000 genomes]
rs73147784	1.00[EUR][1000 genomes]
rs73149516	1.00[EUR][1000 genomes]
rs73818173	1.00[EUR][1000 genomes]
rs7657528	1.00[EUR][1000 genomes]
rs7658546	1.00[EUR][1000 genomes]
rs7660482	1.00[EUR][1000 genomes]
rs7668948	1.00[EUR][1000 genomes]
rs7689472	1.00[EUR][1000 genomes]
rs7691475	1.00[EUR][1000 genomes]
rs7696276	1.00[EUR][1000 genomes]
rs7696283	1.00[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	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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55032400-55039600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:55037000-55038800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:55037800-55038200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:55038000-55038600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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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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