Variant report

Variant	rs1751281
Chromosome Location	chr10:4468804-4468805
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11813500	1.00[AMR][1000 genomes]
rs11815971	1.00[AMR][1000 genomes]
rs11817023	1.00[AMR][1000 genomes]
rs11818101	1.00[AMR][1000 genomes]
rs11819442	1.00[AMR][1000 genomes]
rs1616155	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1679412	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1679432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17132623	1.00[AMR][1000 genomes]
rs17132691	1.00[AMR][1000 genomes]
rs17132695	1.00[AMR][1000 genomes]
rs17132748	1.00[AMR][1000 genomes]
rs17132779	1.00[AMR][1000 genomes]
rs1751278	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1751294	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2478583	1.00[EUR][1000 genomes]
rs74111157	1.00[AMR][1000 genomes]
rs74111159	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894787	chr10:4385379-4857717	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1051290	chr10:4435293-4493026	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv540461	chr10:4435293-4493026	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	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	chr10:4468400-4472400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:4468600-4470200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr10:4468600-4470400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr10:4468600-4470400	Enhancers	NHDF-Ad	bronchial
5	chr10:4468800-4469000	Enhancers	Fetal Lung	lung
6	chr10:4468800-4469200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:4468800-4470600	Enhancers	Adipose Derived Mesenchymal Stem Cell 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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