Variant report

Variant	rs72756333
Chromosome Location	chr9:98459256-98459257
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17299607	0.81[EUR][1000 genomes]
rs17372214	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17372603	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1889207	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2082694	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35864266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72756313	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98458600-98459600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:98458600-98459600	Enhancers	Fetal Intestine Small	intestine
3	chr9:98458600-98459800	Enhancers	Fetal Intestine Large	intestine
4	chr9:98458600-98459800	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr9:98458800-98459600	Enhancers	Duodenum Mucosa	Duodenum
6	chr9:98458800-98459600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr9:98458800-98459600	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr9:98458800-98459800	Enhancers	HepG2	liver
9	chr9:98459000-98459400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:98459200-98460000	ZNF genes & repeats	ES-I3 Cell Line	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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