Variant report

Variant	rs59719366
Chromosome Location	chr10:49830818-49830819
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]
rs1550775	1.00[EUR][1000 genomes]
rs3923678	1.00[EUR][1000 genomes]
rs4114457	0.83[AFR][1000 genomes]
rs58638938	1.00[EUR][1000 genomes]
rs59338484	1.00[EUR][1000 genomes]
rs59868190	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60670300	1.00[EUR][1000 genomes]
rs6537569	1.00[EUR][1000 genomes]
rs7077507	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7081000	1.00[EUR][1000 genomes]
rs7084382	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7084773	1.00[EUR][1000 genomes]
rs7090899	1.00[EUR][1000 genomes]
rs7098132	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74130520	1.00[EUR][1000 genomes]
rs7909038	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7909943	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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 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	chr10:49813400-49844200	Weak transcription	Pancreas	Pancrea
2	chr10:49823400-49832000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr10:49827600-49831600	Weak transcription	NHDF-Ad	bronchial
4	chr10:49828800-49841400	Weak transcription	Aorta	Aorta
5	chr10:49829000-49831200	Weak transcription	Right Atrium	heart
6	chr10:49830800-49831400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr10:49830800-49831600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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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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