Variant report

Variant	rs72810452
Chromosome Location	chr10:61230281-61230282
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11006472	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11006494	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11006526	0.80[ASN][1000 genomes]
rs12412866	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12412878	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12414129	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1450769	0.81[ASN][1000 genomes]
rs1450770	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59927032	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72810421	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72810445	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72810446	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72810488	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv508587	chr10:61150897-61278845	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv895564	chr10:61220923-61327502	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island 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	chr10:61230000-61230600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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