Variant report

Variant	rs74104452
Chromosome Location	chr13:88726400-88726401
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs16962286	1.00[AMR][1000 genomes]
rs16963883	1.00[AMR][1000 genomes]
rs16964065	1.00[AMR][1000 genomes]
rs56203206	1.00[AMR][1000 genomes]
rs56248013	1.00[AMR][1000 genomes]
rs58185871	1.00[AMR][1000 genomes]
rs59150082	1.00[AMR][1000 genomes]
rs59917522	1.00[AMR][1000 genomes]
rs7317093	1.00[AMR][1000 genomes]
rs74103986	1.00[AMR][1000 genomes]
rs74103987	1.00[AMR][1000 genomes]
rs74104001	1.00[AMR][1000 genomes]
rs74104217	1.00[AMR][1000 genomes]
rs74104231	1.00[AMR][1000 genomes]
rs74104239	1.00[AMR][1000 genomes]
rs74104240	1.00[AMR][1000 genomes]
rs74104429	1.00[AMR][1000 genomes]
rs74104436	1.00[AMR][1000 genomes]
rs74104437	1.00[AMR][1000 genomes]
rs74104459	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74104460	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74104465	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74104467	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74106810	1.00[AMR][1000 genomes]
rs74106811	1.00[AMR][1000 genomes]
rs74106812	1.00[AMR][1000 genomes]
rs74107609	1.00[AMR][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	nsv900790	chr13:88585928-88891870	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv900791	chr13:88623302-88771495	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv900792	chr13:88623302-88871759	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv900793	chr13:88711960-88871759	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	2 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	chr13:88726200-88726600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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