Variant report

Variant	rs72796025
Chromosome Location	chr10:58697428-58697429
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10509066	0.83[EUR][1000 genomes]
rs10509067	0.83[EUR][1000 genomes]
rs10509068	0.83[EUR][1000 genomes]
rs11814663	0.83[EUR][1000 genomes]
rs11814678	0.83[EUR][1000 genomes]
rs11816359	0.83[EUR][1000 genomes]
rs11816376	0.83[EUR][1000 genomes]
rs11816789	0.83[EUR][1000 genomes]
rs11816824	0.83[EUR][1000 genomes]
rs12764475	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12764750	0.80[EUR][1000 genomes]
rs12772357	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12775731	0.81[AMR][1000 genomes]
rs12779980	0.88[AMR][1000 genomes]
rs12780982	0.83[EUR][1000 genomes]
rs16909813	0.83[EUR][1000 genomes]
rs16909818	0.83[EUR][1000 genomes]
rs16909819	0.83[EUR][1000 genomes]
rs16909825	0.83[EUR][1000 genomes]
rs16909827	0.83[EUR][1000 genomes]
rs34089772	0.80[EUR][1000 genomes]
rs34133518	0.84[EUR][1000 genomes]
rs34154541	0.85[EUR][1000 genomes]
rs34226604	0.85[EUR][1000 genomes]
rs34396999	0.80[EUR][1000 genomes]
rs34528047	0.80[EUR][1000 genomes]
rs34594186	0.85[EUR][1000 genomes]
rs34995364	0.85[EUR][1000 genomes]
rs35026095	0.85[EUR][1000 genomes]
rs35104970	0.88[AMR][1000 genomes]
rs35791999	0.85[EUR][1000 genomes]
rs35794494	0.80[EUR][1000 genomes]
rs36106545	0.85[EUR][1000 genomes]
rs4540771	0.88[AMR][1000 genomes]
rs61854567	0.80[EUR][1000 genomes]
rs61854597	0.85[EUR][1000 genomes]
rs66486666	0.83[EUR][1000 genomes]
rs66615433	0.88[AMR][1000 genomes]
rs66661996	0.80[EUR][1000 genomes]
rs993745	0.88[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	nsv551064	chr10:58457011-58702440	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv895511	chr10:58640650-58789387	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv895512	chr10:58640650-58834542	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv895513	chr10:58672533-58979792	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	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	chr10:58694600-58698000	ZNF genes & repeats	hESC Derived CD184+ Endoderm 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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