Variant report

Variant	rs72815416
Chromosome Location	chr2:76979685-76979686
allele	A/G
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:16)

rs_ID	r²[population]
rs10165411	0.90[EUR][1000 genomes]
rs10207289	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17404969	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55756601	0.84[EUR][1000 genomes]
rs55799726	0.90[AMR][1000 genomes]
rs56259618	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs60161954	0.89[EUR][1000 genomes]
rs62170445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62170447	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62170448	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62170451	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62172099	0.82[EUR][1000 genomes]
rs62172100	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62172104	0.88[AMR][1000 genomes]
rs72815415	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9917184	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv582235	chr2:76881210-76997763	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv874320	chr2:76971709-77013724	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv458263	chr2:76976626-76994984	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76963800-76985800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:76973400-76989200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr2:76974800-76986600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:76977600-76981800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:76979400-76988200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:76979600-76980600	Enhancers	Fetal Heart	heart

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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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