Variant report

Variant	rs57654746
Chromosome Location	chr2:57164707-57164708
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs13396888	0.89[ASN][1000 genomes]
rs13423943	0.84[ASN][1000 genomes]
rs17048553	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs17048562	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs28497371	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs28599982	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv582059	chr2:56892585-57175087	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv997255	chr2:57043023-57430709	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv998937	chr2:57059299-57357292	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv457963	chr2:57060131-57397423	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv582061	chr2:57060131-57397423	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv470466	chr2:57062513-57397423	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv1004528	chr2:57078722-57182354	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv457974	chr2:57114156-57175087	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv582062	chr2:57114156-57175087	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2754380	chr2:57148349-57306249	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv1000901	chr2:57151366-57193187	Enhancers	n/a	n/a	inside rSNPs	n/a
12	nsv834104	chr2:57151611-57296327	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57164400-57165000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:57164400-57165000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr2:57164400-57165000	Enhancers	iPS-15b 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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