Variant report

Variant	rs57636490
Chromosome Location	chr10:53025631-53025632
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10490976	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16915870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16915935	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16915940	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs57957904	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61295989	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133542	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7901396	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1036645	chr10:52804961-53159076	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv831874	chr10:53010357-53195508	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:53018400-53051200	Weak transcription	Aorta	Aorta
2	chr10:53021200-53028400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr10:53021600-53025800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:53021600-53026200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:53022800-53028400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr10:53023600-53025800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:53023600-53026000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr10:53024600-53026400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr10:53025400-53026600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:53025400-53027000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr10:53025400-53028400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr10:53025400-53030000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr10:53025600-53026000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr10:53025600-53026000	Enhancers	H9 Cell Line	embryonic stem cell
15	chr10:53025600-53026000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr10:53025600-53026800	Enhancers	NHDF-Ad	bronchial

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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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