Variant report

Variant	rs16941700
Chromosome Location	chr15:60032569-60032570
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16941778	1.00[ASN][1000 genomes]
rs16941794	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16941815	1.00[ASN][1000 genomes]
rs35653662	1.00[ASN][1000 genomes]
rs57544209	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57888850	1.00[ASN][1000 genomes]
rs7163881	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7164415	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7164454	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7164568	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7165409	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73433573	0.80[EUR][1000 genomes]
rs8036841	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv984219	chr15:60026752-60043941	Enhancers	Chromatin interactive region	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	chr15:60030000-60034400	Enhancers	Liver	Liver
2	chr15:60030600-60033400	Enhancers	HepG2	liver

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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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