Variant report

Variant	rs72737425
Chromosome Location	chr9:85180587-85180588
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11139608	0.83[AMR][1000 genomes]
rs11139609	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11139610	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11139611	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11139614	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11139615	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11139630	0.91[EUR][1000 genomes]
rs11139631	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11139632	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11139633	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12176641	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12238509	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4146867	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs67169967	0.94[EUR][1000 genomes];0.81[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	nsv831641	chr9:85145561-85309589	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3341772	chr9:85176432-85180630	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85180000-85180600	Enhancers	Rectal Smooth Muscle	rectum
2	chr9:85180000-85181200	Enhancers	Fetal Muscle Leg	muscle
3	chr9:85180000-85181200	Enhancers	Fetal Stomach	stomach
4	chr9:85180200-85180600	Enhancers	Liver	Liver
5	chr9:85180200-85181000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr9:85180200-85181200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:85180200-85181200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:85180200-85181200	Enhancers	Colon Smooth Muscle	Colon
9	chr9:85180400-85180600	Enhancers	Fetal Lung	lung
10	chr9:85180400-85180800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr9:85180400-85180800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr9:85180400-85181000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr9:85180400-85181200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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