Variant report

Variant	rs187018
Chromosome Location	chr21:17606345-17606346
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10211887	1.00[EUR][1000 genomes]
rs1492961	1.00[EUR][1000 genomes]
rs239079	0.83[AMR][1000 genomes]
rs239081	1.00[EUR][1000 genomes]
rs28815621	1.00[EUR][1000 genomes]
rs28816233	1.00[EUR][1000 genomes]
rs41417245	1.00[EUR][1000 genomes]
rs57049577	1.00[AMR][1000 genomes]
rs59959559	1.00[EUR][1000 genomes]
rs7278795	1.00[EUR][1000 genomes]
rs73890803	1.00[EUR][1000 genomes]
rs73893217	1.00[EUR][1000 genomes]
rs73893218	1.00[EUR][1000 genomes]
rs8129609	1.00[EUR][1000 genomes]
rs9974249	1.00[EUR][1000 genomes]
rs9975033	0.85[AMR][1000 genomes]
rs9976640	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432145	chr21:17559229-17628529	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv834051	chr21:17564843-17721764	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17584400-17619400	Weak transcription	Hela-S3	cervix
2	chr21:17585000-17612200	Weak transcription	Adipose Nuclei	Adipose
3	chr21:17598000-17622200	Weak transcription	Ovary	ovary
4	chr21:17598000-17622400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr21:17602000-17614000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr21:17603000-17608000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr21:17604200-17607400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr21:17606000-17612000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr21:17606200-17622200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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