Variant report

Variant	rs60813730
Chromosome Location	chr2:76990961-76990962
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10202468	1.00[EUR][1000 genomes]
rs10209686	1.00[EUR][1000 genomes]
rs10209803	1.00[EUR][1000 genomes]
rs11896684	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11901875	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13382600	1.00[EUR][1000 genomes]
rs13385215	1.00[EUR][1000 genomes]
rs13389599	1.00[EUR][1000 genomes]
rs13402128	1.00[EUR][1000 genomes]
rs13405495	1.00[EUR][1000 genomes]
rs13429829	1.00[EUR][1000 genomes]
rs13431330	1.00[EUR][1000 genomes]
rs59328315	1.00[EUR][1000 genomes]
rs6733240	1.00[EUR][1000 genomes]
rs72917793	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72919613	1.00[AMR][1000 genomes]
rs72919625	1.00[EUR][1000 genomes]
rs7595825	0.89[AMR][1000 genomes]
rs7595836	1.00[EUR][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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76988000-76998400	Weak transcription	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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