Variant report

Variant	rs62170447
Chromosome Location	chr2:76988627-76988628
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:16)

rs_ID	r²[population]
rs10165411	0.92[EUR][1000 genomes]
rs10207289	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17404969	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55756601	0.86[EUR][1000 genomes]
rs55799726	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56259618	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs60161954	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62170445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62170448	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62170451	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62172099	0.84[EUR][1000 genomes]
rs62172100	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62172104	0.88[AMR][1000 genomes]
rs72815415	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72815416	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9917184	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
4	nsv1011401	chr2:76982546-77068714	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76973400-76989200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:76987600-76989000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:76988000-76989000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:76988000-76998400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:76988200-76990400	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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