Variant report

Variant	rs74082096
Chromosome Location	chr13:62547642-62547643
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs57938780	1.00[AMR][1000 genomes]
rs7322813	1.00[AMR][1000 genomes]
rs73488482	1.00[AMR][1000 genomes]
rs73488793	1.00[AMR][1000 genomes]
rs73488796	1.00[AMR][1000 genomes]
rs73490745	1.00[AMR][1000 genomes]
rs73490780	1.00[AMR][1000 genomes]
rs73494809	1.00[AMR][1000 genomes]
rs73494814	1.00[AMR][1000 genomes]
rs73494815	1.00[AMR][1000 genomes]
rs73494818	1.00[AMR][1000 genomes]
rs73499061	1.00[AMR][1000 genomes]
rs73499070	1.00[AMR][1000 genomes]
rs73502870	1.00[AMR][1000 genomes]
rs73505018	1.00[AMR][1000 genomes]
rs73505035	1.00[AMR][1000 genomes]
rs73505036	1.00[AMR][1000 genomes]
rs7986197	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761266	chr13:61928642-62690828	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1038867	chr13:62302878-62594554	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv900251	chr13:62502166-62624458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv900252	chr13:62502166-62687843	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv900253	chr13:62515266-62660299	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:62547200-62548400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr13:62547400-62548200	Enhancers	hESC Derived CD56+ Ectoderm 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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