Variant report

Variant	rs36036528
Chromosome Location	chr3:53665019-53665020
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13059151	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13084908	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1380608	0.86[AFR][1000 genomes]
rs2946522	0.97[EUR][1000 genomes]
rs34804225	0.86[AFR][1000 genomes]
rs35768922	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35989759	0.92[EUR][1000 genomes]
rs3774487	0.98[EUR][1000 genomes]
rs3774488	0.98[EUR][1000 genomes]
rs3774490	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3774496	0.97[EUR][1000 genomes]
rs3774503	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3821853	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs66596667	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71301841	0.89[ASN][1000 genomes]
rs71301844	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71301850	0.86[AFR][1000 genomes]
rs73840150	1.00[ASN][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	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53652800-53684000	Weak transcription	Right Atrium	heart
2	chr3:53661400-53667200	Weak transcription	Fetal Intestine Large	intestine
3	chr3:53662000-53665400	Enhancers	Stomach Mucosa	stomach
4	chr3:53664000-53668600	Weak transcription	Gastric	stomach
5	chr3:53664200-53665200	Weak transcription	Fetal Lung	lung
6	chr3:53664400-53665200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr3:53665000-53665200	Enhancers	Esophagus	oesophagus
8	chr3:53665000-53665200	ZNF genes & repeats	Fetal Intestine Small	intestine
9	chr3:53665000-53665200	Enhancers	Pancreas	Pancrea
10	chr3:53665000-53667600	Weak transcription	HepG2	liver

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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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