Variant report

Variant	rs58800905
Chromosome Location	chr5:57962448-57962449
allele	C/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]
rs1019470	1.00[EUR][1000 genomes]
rs16888343	1.00[EUR][1000 genomes]
rs16888349	1.00[EUR][1000 genomes]
rs60640515	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73759508	1.00[EUR][1000 genomes]
rs73759510	1.00[EUR][1000 genomes]
rs73759513	1.00[EUR][1000 genomes]
rs73759514	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73759515	0.97[AFR][1000 genomes]
rs73759528	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73759529	1.00[EUR][1000 genomes]
rs73759530	1.00[EUR][1000 genomes]
rs73759531	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];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	esv2830363	chr5:57893949-58555491	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1029145	chr5:57905821-58141221	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830311	chr5:57912546-58105636	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv4845	chr5:57949493-57994156	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57961800-57963000	Weak transcription	Stomach Mucosa	stomach
2	chr5:57961800-57967400	Enhancers	HUVEC	blood vessel
3	chr5:57962200-57962600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:57962200-57963200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:57962400-57962600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr5:57962400-57963400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:57962400-57963400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:57962400-57963400	Enhancers	Primary hematopoietic stem cells	blood
9	chr5:57962400-57963400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:57962400-57964000	Enhancers	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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